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Myophosphorylase deficiency (McArdle's disease) in two interrelated families

The clinical and laboratory findings are presented of three patients (two affected sisters and their male cousin) with myophosphorylase deficiency in two interrelated families. Nine unaffected relatives were also investigated. Although the three patients demonstrated the characteristic features of t...

詳細記述

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書誌詳細
主要な著者: Cochrane, P., Hughes, R. R., Buxton, P. H., Yorke, R. A.
フォーマット: Artigo
言語:Inglês
出版事項: 1973
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1083557/
https://ncbi.nlm.nih.gov/pubmed/4513544
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