Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families (Q72017458)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

title

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference

Fontaine B

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Vale-Santos J

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Jurkat-Rott K

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Reboul J

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Plassart E

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Rime CS

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Elbaz A

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Heine R

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Guimarães J

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Weissenbach J

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

publication date

1 March 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

number of pages

6

1 reference

inferred from page(s)

published in

Nature Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

volume

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

page(s)

267-272

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/ng0394-267

22 October 2019

exact match

0 references

cites work

A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Temperature-sensitive mutations in the III–IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

A novel SCN4A mutation causing myotonia aggravated by cold and potassium

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Functional expression of sodium channel mutations identified in families with periodic paralysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Functional consequences of a Na+ channel mutation causing hyperkalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

The skeletal muscle chloride channel in dominant and recessive human myotonia

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Permanent muscle weakness in familial hypokalaemic periodic paralysis. Clinical, radiological and pathological aspects.

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Hypokalemic periodic paralysis: In vitro investigation of muscle fiber membrane parameters

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Different gene loci for hyperkalemic and hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Exclusion of linkage between hypokalemic periodic paralysis (HOKPP) and three candidate loci

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

A second-generation linkage map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Assignment of the human gene for the alpha 1 subunit of the skeletal muscle DHP-sensitive Ca2+ channel (CACNL1A3) to chromosome 1q31-q32

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Genomic organization, nucleotide sequence, and cellular distribution of a Shaw-related potassium channel gene, Kv3.3, and mapping of Kv3.3 and Kv3.4 to human chromosomes 19 and 1

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

The CEPH consortium linkage map of human chromosome 1

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

A PCR-based linkage map of human chromosome 1.

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Chromosome mapping of five human cardiac and skeletal muscle sarcoplasmic reticulum protein genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Exclusion of malignant hyperthermia susceptibility (MHS) from a putative MHS2 locus on chromosome 17q and of the alpha 1, beta 1, and gamma subunits of the dihydropyridine receptor calcium channel as candidates for the molecular defect

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Genetic mapping of the beta 1- and gamma-subunits of the human skeletal muscle L-type voltage-dependent calcium channel on chromosome 17q and exclusion as candidate genes for malignant hyperthermia susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

DNA polymorphism and human disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-267

7 January 2021

Identifiers

DOI

10.1038/NG0394-267

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8012389%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference