Non-lethal congenital hypotonia due to glycogen storage disease type IV-Reference-Cited by-同舟云学术

Non-lethal congenital hypotonia due to glycogen storage disease type IV

Published:2006-04-15 Issue:8 Volume:140A Page:878-882
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Burrow T. Andrew,Hopkin Robert J.,Bove Kevin E.,Miles Lili,Wong Brenda L.,Choudhary Arabinda,Bali Deeksha,Li Sing Chung,Chen Yuan-Tsong

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference18 articles.

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2. Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene.

3. A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy

4. Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV)

5. 2001. Glycogen storage diseases. In: , , , , , , editors. The metabolic and molecular bases of inherited disease. New York: McGraw Hill. p 1521–1551.

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