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Neuromuscular Disorders : NMD|March 15, 2006
'Cap myopathy': case report of a familyJ M Cuisset, C A Maurage, J F Pellissier, et al.Neurology|December 3, 2008
New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutationsM Ohlsson, S Quijano-Roy, N Darin, et al.European Journal of Neurology|March 3, 2018
Ryanodine receptor type 3 (RYR3) as a novel gene associated with a myopathy with nemaline bodiesY Nilipour, S Nafissi, A E Tjust, et al.Pageof 2