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Debrancher Enzyme Activity in Blood Cells of Families with Type III Glycogen Storage Disease. A Method for Diagnosis of Heterozygotes

Overview
Journal Isr J Med Sci
Specialty General Medicine
Date 1967 May 1
PMID 5317552
Citations 4
Authors
R Chayoth
S W Moses
K Steinitz
Affiliations
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X-chromosomal inheritance of liver glycogenosis with phosphorylase kinase deficiency.

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Moses S, Chayoth R, Levin S, Lazarovitz E, Rubinstein D J Clin Invest. 1968; 47(6):1343-8.

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Myopathies due to enzyme deficiencies.

Cornelio F, Di Donato S J Neurol. 1985; 232(6):329-40.

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