✦ LIBER ✦
C.P.3.03 Novel POMT2 mutations associated with a marked reduction of POMT activity causing congenital muscular dystrophy with mental retardation and microcephaly
✍ Scribed by A. Yanagisawa; C. Bouchet; H. Manya; S. Quijano-Roy; P. van den Bergh; L. Viollet; J. Cuisset; F. Leturcq; N. Romero; M. Fardeau; N. Seta; T. Endo; P. Guicheney
- Book ID
- 116793211
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 50 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0960-8966
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