FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients. Issue 4 (1st April 2004)

• Record Type: Journal Article
• Authors: Walter, M C; Petersen, J A; Stucka, R; Fischer, D; Schröder, R; Vorgerd, M; Schroers, A; Schreiber, H; Hanemann, C O; Knirsch, U; Rosenbohm, A; Huebner, A; Barisic, N; Horvath, R; Komoly, S; Reilich, P; Müller-Felber, W; Pongratz, D; Müller, J S; Auerswald, E A; Lochmüller, H
• Is Part Of: Journal of medical genetics. Volume 41:Issue 4(2004)
• Page Start: e50
• Page End: e50
• Publication Date: 2004-04-01
• Subjects: common mutation Leu276Ile -- 826C>A change -- FKRP -- LGMD2I; DAG, dystrophin-associated-glycoprotein complex -- FKRP, fukutin-related protein -- LGMD, limb-girdle muscular dystrophy -- MDC, congenital muscular dystrophy; Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmg.2003.013953
• Languages: English
• ISSNs: 1468-6244