A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvement
Titel:
A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvement
Auteur:
Gonzalez-Quereda, Lidia Gallardo, Eduard Töpf, Ana Alonso-Jimenez, Alicia Straub, Volker Rodriguez, Maria Jose Lleixa, Cinta Illa, Isabel Gallano, Pia Diaz-Manera, Jordi