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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...

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Autors principals: Cochrane, P., Hughes, R. R., Buxton, P. H., Yorke, R. A.
Format: Artigo
Idioma:Inglês
Publicat: 1973
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1083557/
https://ncbi.nlm.nih.gov/pubmed/4513544
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