Literature DB >> 5904467

Hepatic phosphorylase defect. Studies on peripheral blood.

P G Wallis, J B Sidbury, R C Harris.   

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Year:  1966        PMID: 5904467     DOI: 10.1001/archpedi.1966.02090060088008

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


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  4 in total

1.  Rare McArdle disease locus polymorphic site on 11q13 contains CpG sequence.

Authors:  R V Lebo; L A Anderson; S DiMauro; E Lynch; P Hwang; R Fletterick
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

2.  Enzyme studies on white blood cells and their significance for genetics.

Authors:  R Wagner
Journal:  Indian J Pediatr       Date:  1971-03       Impact factor: 1.967

3.  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

4.  Phosphorylase kinase deficiency.

Authors:  F Huijing
Journal:  Biochem Genet       Date:  1970-02       Impact factor: 1.890

  4 in total

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