APA

Reilich P., Krause S., Schramm N., Klutzny U., Bulst S., Zehetmayer B., Schneiderat P., Walter M. C., Schoser B. & Lochmüller H. (20111212). A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A). : Journal of neurology.

Chicago

Reilich Peter, Krause Sabine, Schramm Nicolai, Klutzny Ursula, Bulst Stefanie, Zehetmayer Barbara, Schneiderat Peter, Walter Maggie C, Schoser Benedikt and Lochmüller Hanns. 20111212. A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A). : Journal of neurology.

Harvard

Reilich P., Krause S., Schramm N., Klutzny U., Bulst S., Zehetmayer B., Schneiderat P., Walter M. C., Schoser B. and Lochmüller H. (20111212). A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A). : Journal of neurology.

MLA

Reilich Peter, Krause Sabine, Schramm Nicolai, Klutzny Ursula, Bulst Stefanie, Zehetmayer Barbara, Schneiderat Peter, Walter Maggie C, Schoser Benedikt and Lochmüller Hanns. A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A). : Journal of neurology. 20111212.