Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype

✍ Scribed by E. Ricci; G. Galluzzi; G. Deidda; S. Cacurri; L. Colantoni; B. Merico; N. Piazzo; S. Servidei; E. Vigneti; V. Pasceri; G. Silvestri; M. Mirabella; F. Mangiola; P. Tonali; L. Felicetti

• Publisher: John Wiley and Sons
• Year: 1999
• Tongue: English
• Weight: 272 KB
• Volume: 45
• Category: Article
• ISSN: 0364-5134
• DOI: 10.1002/1531-8249(199906)45:6<751::aid-ana9>3.0.co;2-m