Molecular Analysis of Glycogen Storage Disease Type Ib: Identification of a Prevalent Mutation among Japanese Patients and Assignment of a Putative Glucose-6-Phosphate Translocase Gene to Chromosome 11-Reference-Cited by-同舟云学术

Molecular Analysis of Glycogen Storage Disease Type Ib: Identification of a Prevalent Mutation among Japanese Patients and Assignment of a Putative Glucose-6-Phosphate Translocase Gene to Chromosome 11

Published:1998-07 Issue:2 Volume:248 Page:426-431
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Kure Shigeo,Suzuki Yoichi,Matsubara Yoichi,Sakamoto Osamu,Shintaku Haruo,Isshiki Gen,Hoshida Chiharu,Izumi Isho,Sakura Nobuo,Narisawa Kuniaki

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference17 articles.

1. The Metabolic and Molecular Bases of Inherited Disease;Chen,1995

2. Mutations in the Glucose-6-Phosphatase Gene that Cause Glycogen Storage Disease Type 1a

3. Identification of mutations in the gene for glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1a.

4. Neutropenia and impaired neutrophil migration in type IB glycogen storage disease

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