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Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene

✍ Scribed by Haiyan Zhou; Suzanne Lillis; Ryan E. Loy; Farshid Ghassemi; Michael R. Rose; Fiona Norwood; Kerry Mills; Safa Al-Sarraj; Russell J.M. Lane; Lucy Feng; Emma Matthews; Caroline A. Sewry; Stephen Abbs; Stefan Buk; Michael Hanna; Susan Treves; Robert T. Dirksen; Gerhard Meissner; Francesco Muntoni; Heinz Jungbluth

Book ID: 116794350
Publisher: Elsevier Science
Year: 2010
Tongue: English
Weight: 924 KB
Volume: 20
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2009.12.005

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