Family with centronuclear myopathy as a result of a novel p.R369G DNM2 mutation

Publisher： John Wiley & Sons Inc

E-ISSN： 2049-4173|3|4|161-162

ISSN： 2049-4173

Source： Neurology And Clinical Neuroscience (Electronic), Vol.3, Iss.4, 2015-07, pp. : 161-162

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Abstract

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