Novel fukutin mutations in limb-girdle muscular dystrophy type 2M with childhood onset.

Smogavec M1, Zschüntzsch J1, Kress W1, Mohr J1, Hellen P1, Zoll B1, Pauli S1, Schmidt J1.
  1. Institute of Human Genetics (M.S., B.Z., S.P.), Department of Neurology (J.Z., J.S.), and Department of Neuroradiology (P.H.), University Medical Center Göttingen; Department of Human Genetics (W.K.), University of Würzburg; and CeGaT GmbH und Praxis für Humangenetik (J.M.), Tübingen, Germany.