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G.P.126 “Strongman syndrome”: A new autosomal dominant herculean painful myopathy

✍ Scribed by Al-Bustani, N.; Tétreault, M.; Provost, S.; Bolduc, V.; Srour, M.; O’Ferrall, E.K.; Dubé, M.P.; Bouchard, J.P.; Ravenscroft, G.; Laing, N.G.; Bignell, D.; Lamont, P.J.; Mathieu, J.; Brais, B.


Book ID
119333958
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
52 KB
Volume
22
Category
Article
ISSN
0960-8966

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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