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P.9.9 A novel de novo mutation in ACTA1 causes a congenital myopathy with misleading type 1 fiber predominance and a peculiar MRI

✍ Scribed by Castiglioni, C.; Cassandrini, D.; Fattori, F.; Bellacchio, E.; Alvarez, K.; D’Amico, A.; Gejman, R.; Díaz, J.; Santorelli, F.M.; Bevilacqua, J.A.; Bertini, E.

Book ID: 123188749
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 47 KB
Volume: 23
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2013.06.522

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