Congenital muscular dystrophy with laminin α2 chain deficiency: Identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry

✍ Scribed by R. Herrmann; V. Straub; K. Meyer; T. Kahn; M. Wagner; T. Voit

• Book ID: 105525423
• Publisher: Springer
• Year: 1996
• Tongue: English
• Weight: 978 KB
• Volume: 155
• Category: Article
• ISSN: 0340-6997
• DOI: 10.1007/bf02282889