| Literature DB >> 8983689 |
D P Nicholls1, N P Campbell, H P Stevenson, V H Patterson.
Abstract
McArdle's disease (myophosphorylase deficiency) results in the inability to metabolise skeletal muscle glycogen to lactate. A patient with this condition developed angina and therefore offered a unique opportunity to explore the differential expression of the defective myophosphorylase gene in skeletal and cardiac muscle.Entities:
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Year: 1996 PMID: 8983689 PMCID: PMC484554 DOI: 10.1136/hrt.76.4.372
Source DB: PubMed Journal: Heart ISSN: 1355-6037 Impact factor: 5.994