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G.P.13.09 Identification of a point mutation in the skeletal muscle ryanodine receptor gene associated in the homozygous state to central core disease

✍ Scribed by G. Melli; L. Colleoni; P. Bernasconi; S. Romaggi; V. Tegazzin; R. Mantegazza; L. Morandi

Book ID: 116793705
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 61 KB
Volume: 18
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2008.06.294

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