A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutations
Titel:
A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutations
Auteur:
Wallace, Stephanie E. Conta, Jessie H. Winder, Thomas L. Willer, Tobias Eskuri, Jamie M. Haas, Richard Patterson, Kathleen Campbell, Kevin P. Moore, Steven A. Gospe Jr., Sidney M.