The clinical diagnosis of McArdle's disease. Identification of another family with deficiency of muscle phosphorylase.
D000328:Adult; D004796:Clinical Enzyme Tests; D006008:Glycogen Storage Disease / Q000235:genetics*; D006801:Humans; D008297:Male; D009135:Muscular Diseases / Q000235:genetics*; D009212:Myoglobinuria / Q000235:genetics*; D010764:Phosphorylase Kinase