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Affected members showed absence of phosphorylase enzyme by histochemical and quantitative estimation. No quantitative abnormalities were found in other enzyme systems of glycolytic pathways in the family investigated. Various other aspects of clinical features, biochemical abnormalities and inheritance are discussed.<\/jats:p>","DOI":"10.1017\/s0317167100025701","type":"journal-article","created":{"date-parts":[[2016,7,28]],"date-time":"2016-07-28T11:32:04Z","timestamp":1469705524000},"page":"175-179","source":"Crossref","is-referenced-by-count":1,"title":["Myophosphorylase Deficiency (McArdle's Disease): Report of a Family"],"prefix":"10.1017","volume":"3","author":[{"given":"M. Zafar","family":"Mahmud","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R. 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