Glycogen storage disease type III with muscle involvement: Reappraisal of phenotypic variability and prognosis-Reference-Cited by-同舟云学术

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Glycogen storage disease type III with muscle involvement: Reappraisal of phenotypic variability and prognosis

Published:1992-03-01 Issue:5 Volume:42 Page:696-699
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Momoi Toru,Sano Hirohiko,Yamanaka Chutaro,Sasaki Hiroshi,Mikawa Haruki

Publisher

Wiley

Subject

Genetics(clinical)

Reference30 articles.

1. Type III Glycogenosis

2. Clinical Varieties of Neuromuscular Disease in Debrancher Deficiency

3. Debrancher deficiency: Neuromuscular disorder in 5 adults

4. Type III glycogenosis presenting as liver disease in adults with atypical histological features.

5. (1989) The glycogen storage disease. In (eds), “The Metabolic Basis of Inherited Disease.” 6th ed. New York, McGraw-Hill Book Co., pp 425-452.

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3. Novel autophagic vacuolar myopathies: Phenotype and genotype features;Neuropathology and Applied Neurobiology;2021-02

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