A common founder for amyotrophic lateral sclerosis type 8 (ALS8) in the Brazilian population (Q58477886)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

A common founder for amyotrophic lateral sclerosis type 8 (ALS8) in the Brazilian population (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

7 January 2020

main subject

0 references

amyotrophic lateral sclerosis type 8

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Ammar Al-Chalabi

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

3

Mayana Zatz

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

publication date

27 September 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

volume

118

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

issue

3-4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

page(s)

499-500

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00439-005-0031-y

7 January 2020

exact match

0 references

cites work

Autosomal dominant late adult spinal muscular atrophy, type Finkel

1 reference

12 December 2020

Estimating the age of rare disease mutations: the example of Triple-A syndrome.

1 reference

12 December 2020

D90A-SOD1 mediated amyotrophic lateral sclerosis: a single founder for all cases with evidence for a Cis-acting disease modifier in the recessive haplotype

1 reference

12 December 2020

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis

1 reference

12 December 2020

Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor

1 reference

12 December 2020

10.1007/S00439-005-0031-Y

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16187141%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference