A novelMYH2mutation in family members presenting with...

Journal of Neurology 2016 / 7 Vol. 263; Iss. 7

A novelMYH2mutation in family members presenting with congenital myopathy, ophthalmoplegia and facial weakness

Willis, Tracey, Hedberg-Oldfors, Carola, Alhaswani, Zoya, Kulshrestha, Richa, Sewry, Caroline, Oldfors, Anders
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Volume:
263
Language:
english
Journal:
Journal of Neurology
DOI:
10.1007/s00415-016-8154-8
Date:
July, 2016
File:
PDF, 1.68 MB
english, 2016
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