(Q35762781)

10 August 2017

title

G to A polymorphism in the second exon of the BCL2 gene (English)

1 reference

10 August 2017

Tanaka S

1

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10 August 2017

Kant J

series ordinal

2

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10 August 2017

Reed JC

series ordinal

3

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10 August 2017

language of work or name

English

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publication date

1 April 1991

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10 August 2017

published in

Nucleic Acids Research

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10 August 2017

volume

19

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10 August 2017

issue

8

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10 August 2017

page(s)

1964

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A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria

10 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328156

One-sided polymerase chain reaction: the amplification of cDNA.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328156

Direct detection of point mutations by mismatch analysis: application to haemophilia B.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328156

Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I)

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328156

Cloning and expression of the cDNA encoding human fumarylacetoacetate hydrolase, the enzyme deficient in hereditary tyrosinemia: assignment of the gene to chromosome 15

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=328156

2 October 2017

Identifiers

DOI

10.1093/NAR/19.8.1964-A

1 reference

10 August 2017

1 reference

10 August 2017

1 reference