Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

✍ Scribed by Piccolo, F.; Roberds, S.L.; Jeanpierre, M.; Leturcq, F.; Azibi, K.; Beldjord, C.; Carrié, A.; Récan, D.; Chaouch, M.; Reghis, A.

• Book ID: 109916259
• Publisher: Nature Publishing Group
• Year: 1995
• Tongue: English
• Weight: 387 KB
• Volume: 10
• Category: Article
• ISSN: 1061-4036
• DOI: 10.1038/ng0695-243