C.P.1.03 TPM3 is a recurrent cause of congenital fibre type disproportion and is associated with a consistent phenotype

✍ Scribed by N. Clarke; H. Kolski; D. Dye; E. Lim; R. Smith; R. Patel; M. Fahey; N. Laing; K. North

• Book ID: 116793097
• Publisher: Elsevier Science
• Year: 2007
• Tongue: English
• Weight: 63 KB
• Volume: 17
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2007.06.248