(Q35247186)

7 August 2017

title

Branching enzyme activity of cultured amniocytes and chorionic villi: prenatal testing for type IV glycogen storage disease (English)

1 reference

7 August 2017

1 reference

Brown BI

1

1 reference

7 August 2017

Brown DH

series ordinal

2

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 March 1989

1 reference

American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

44

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7 August 2017

issue

3

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7 August 2017

page(s)

378-381

1 reference

Familial cirrhosis of the liver with storage of abnormal glycogen

7 August 2017

cites work

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715438

Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis

12 July 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715438

Studies on leukocyte brancher enzyme activityin a family with type IV glycogenosis

12 July 2018

1 reference

12 December 2020

A rapid filter paper assay for UDPglucose-glycogen glucosyltransferase, including an improved biosynthesis of UDP-14C-glucose

1 reference

12 December 2020

Studies of the residual glycogen branching enzyme activity present in human skin fibroblasts from patients with Type IV glycogen storage disease

1 reference

12 December 2020

Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotes

1 reference

12 December 2020

Structure of glycogens and amylopectins. III. Normal and abnormal human glycogen

1 reference

12 December 2020

Type IV glycogen storage disease: branching enzyme deficiency in skin fibroblasts and possible heterozygote detection

1 reference

12 December 2020

Identifiers

PMC publication ID

1715438

1 reference

7 August 2017

1 reference