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Autosomal Dominant Partial Epilepsy with Auditory Features: Description of a New Family

✍ Scribed by R. Michelucci; D. Passarelli; S. Pitzalis; G. Dal Corso; C. A. Tassinari; C. Nobile


Book ID
109108204
Publisher
Wiley (Blackwell Publishing)
Year
2000
Tongue
English
Weight
332 KB
Volume
41
Category
Article
ISSN
0013-9580

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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