A new de novo missense mutation in MYH2 expands clinical...

A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathies

D’Amico, A., Fattori, F., Bellacchio, E., Catteruccia, M., Servidei, S., Bertini, E.

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Volume:

Language:

english

Journal:

Neuromuscular Disorders

DOI:

10.1016/j.nmd.2013.02.011

Date:

May, 2013

File:

PDF, 506 KB

english, 2013

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