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

✍ Scribed by D’Amico, A.; Fattori, F.; Bellacchio, E.; Catteruccia, M.; Servidei, S.; Bertini, E.

Book ID: 122574020
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 506 KB
Volume: 23
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2013.02.011

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