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P3.41. Clinical and genetic findings in a large cohort of patients with congenital myopathies due to mutations in the skeletal muscle ryanodine receptor (RYR1) gene

✍ Scribed by A. Klein; S. Lillis; I. Oprea; M. Scoto; S. Robb; A. Manzur; V. Straub; H. Roper; P.Y. Jeannet; H. Kingston; U.B. Jensen; E. Wraige; N. Trump; W. Rakowicz; M. Roberts; C. Longman; H. Lochmuller; K. Bushby; M.I. Hughes; S. Abbs; H. Jungbluth; F. Muntoni

Book ID: 116795117
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 49 KB
Volume: 21
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2011.06.935

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