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Familial centronuclear myopathy: a clinical and pathological study

✍ Scribed by E. Reske-Nielsen; O. Hein-ßrensen; P. Vorre

Book ID
114782418
Publisher
John Wiley and Sons
Year
1987
Tongue
English
Weight
650 KB
Volume
76
Category
Article
ISSN
0001-6314

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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