Sequence variations in the first exon of alpha-galactosidase A. (Q33595678)

28 July 2017

title

Sequence variations in the first exon of alpha-galactosidase A. (English)

1 reference

28 July 2017

Davies JP

1

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28 July 2017

Winchester BG

series ordinal

2

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28 July 2017

Malcolm S

series ordinal

3

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28 July 2017

language of work or name

English

0 references

publication date

1 August 1993

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

30

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28 July 2017

issue

8

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28 July 2017

page(s)

658-663

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Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

28 July 2017

cites work

1 reference

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A simple salting out procedure for extracting DNA from human nucleated cells

21 June 2018

1 reference

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An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

21 June 2018

1 reference

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Synthesis and processing of alpha-galactosidase A in human fibroblasts. Evidence for different mutations in Fabry disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

Human alpha-galactosidase A: nucleotide sequence of a cDNA clone encoding the mature enzyme

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

Fabry disease: isolation of a cDNA clone encoding human alpha-galactosidase A

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

Anderson Fabry disease, a close linkage with highly polymorphic DNA markers DXS17, DXS87 and DXS88.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

Structural organization of the human alpha-galactosidase A gene: further evidence for the absence of a 3' untranslated region

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

Nucleotide sequence of the human alpha-galactosidase A gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

Fabry disease: six gene rearrangements and an exonic point mutation in the alpha-galactosidase gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

Identification of point mutations in the alpha-galactosidase A gene in classical and atypical hemizygotes with Fabry disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

A case of Fabry's disease in a patient with no alpha-galactosidase A activity caused by a single amino acid substitution of Pro-40 by Ser

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI site

21 June 2018

1 reference

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An Atypical Variant of Fabry's Disease with Manifestations Confined to the Myocardium

21 June 2018

1 reference

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Polymorphisms in the transcribed 3' untranslated region of eukaryotic genes

21 June 2018

1 reference

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

21 June 2018

1 reference

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AhaII polymorphism in human X-linked proteolipid protein gene (PLP)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

Fabry disease in a large Nova Scotia kindred: carrier detection using leucocyte alpha-galactosidase activity and an NcoI polymorphism detected by an alpha-galactosidase cDNA clone

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

Point mutations in the upstream region of the ?-galactosidase A gene exon 6 in an atypical variant of Fabry disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

Anderson‐fabry disease: Rapid detection of carriers by hair bulb analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016494

Fabry's disease: enzymatic diagnosis of hemizygotes and heterozygotes. Alpha-galactosidase activities in plasma, serum, urine, and leukocytes

21 June 2018

1 reference

12 December 2020

Fabry disease: molecular diagnosis of hemizygotes and heterozygotes

1 reference

12 December 2020

A 3′ splice site consensus sequence mutation in the intron 3 of the α-galactosidase a gene in a patient with Fabry disease

1 reference

12 December 2020

Invariant exon skipping in the human α-galactosidase A pre-mRNA: A g+1 to t substitution in a 5′-splice site causing Fabry disease

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.30.8.658

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28 July 2017

1 reference

28 July 2017

1 reference