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P1.24 Mutations in ANO5 represent a common cause of non-dysferlin LGMD2B and Miyoshi myopathy

✍ Scribed by D. Hicks; A. Sarkozy; N. Muelas; A. Huebner; G. Hudson; R. Barresi; J. Miller; J. Gowers; P.J. Hughes; R. Roberts; D. Turnbull; S. Krause; M. Walter; S. Laval; V. Straub; H. Lochmüller; K. Bushby


Book ID
116794469
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
37 KB
Volume
20
Category
Article
ISSN
0960-8966

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