Myofibrillar activation failure in McArdle's disease
β Scribed by Robert G. Cooper; Maria J. Stokes; Richard H.T. Edwards
- Book ID
- 118930815
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 512 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0022-510X
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## Abstract Inherited deficiency of myophosphorylase leads to glycogen storage disease type V (McArdle's disease). We performed mutation analysis in 9 patients of eight unrelated families from Germany with typical cliniclal presentation of myophosβphorylase deficiency. Beside previously described m