Molecular biology and gene therapy for glycogen storage disease type Ib-Reference-Cited by-同舟云学术

Molecular biology and gene therapy for glycogen storage disease type Ib

Published:2018-04-16 Issue:6 Volume:41 Page:1007-1014
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Chou Janice Y.¹^ORCID,Cho Jun-Ho¹,Kim Goo-Young¹,Mansfield Brian C.¹²

Affiliation:

1. ; Section on Cellular Differentiation, Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institutes of Health; Building 10, Room 8N240C, NIH 10 Center Drive Bethesda MD 20892-1830 USA

2. ; Foundation Fighting Blindness; Columbia MD 21046 USA

Funder

Intramural Research Program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institutes of Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/article/10.1007/s10545-018-0180-5/fulltext.html

Reference59 articles.

1. The gene for glycogen-storage disease type 1b maps to chromosome 11q23;Annabi;Am J Hum Genet,1998

2. A clinical and molecular review of ubiquitous glucose-6-phosphatase deficiency caused by G6PC3 mutations;Banka;Orphanet J Rare Dis,2013

3. Liver transplantation in glycogen storage disease type I;Boers;Orphanet J Rare Dis,2014

4. A syndrome with congenital neutropenia and mutations in G6PC3;Boztug;N Engl J Med,2009

5. Recombinant human granulocyte colony-stimulating factor therapy for patients with neutropenia and/or neutrophil dysfunction secondary to glycogen storage disease type 1b;Calderwood;Blood,2001

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