Autosomal dominant centronuclear myopath
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Kevin J. Felice; Margaret L. Grunnet
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Article
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1997
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John Wiley and Sons
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English
β 304 KB
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The centronuclear myopathies are a clinically and genetically heterogeneous group of disorders which share similar histological features on muscle biopsy. The familial cases have been classified genetically as X-linked or autosomal in inheritance. The autosomal forms usually have a later onset and m