Literature DB >> 5317552

Debrancher enzyme activity in blood cells of families with type III glycogen storage disease. A method for diagnosis of heterozygotes.

R Chayoth, S W Moses, K Steinitz.   

Abstract

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Year:  1967        PMID: 5317552

Source DB:  PubMed          Journal:  Isr J Med Sci        ISSN: 0021-2180


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  3 in total

1.  X-chromosomal inheritance of liver glycogenosis with phosphorylase kinase deficiency.

Authors:  F Huijing; J Fernandes
Journal:  Am J Hum Genet       Date:  1969-05       Impact factor: 11.025

2.  Myopathies due to enzyme deficiencies.

Authors:  F Cornelio; S Di Donato
Journal:  J Neurol       Date:  1985       Impact factor: 4.849

3.  Glucose and glycogen metabolism in erythrocytes from normal and glycogen storage disease type III subjects.

Authors:  S W Moses; R Chayoth; S Levin; E Lazarovitz; D Rubinstein
Journal:  J Clin Invest       Date:  1968-06       Impact factor: 14.808

  3 in total

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