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Article

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

13 Mar 2013

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Share to Cardiomyopathy and Myosin Studies
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 23489661
DOI: 10.1016/j.nmd.2013.02.011

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