The phenotype of chromosome 2p-linked limb-girdle muscular dystrophy

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

Isabelle Richard, Odile Broux, Valéerie Allamand et al. · Cell · 1995 · 997 citations · Full text

Life Sciences, Genetics, Molecular Biology +11

Disorders of Voluntary Muscle

The Medical Journal of Australia · 1965 · 591 citations

Medicine, Anatomy, Neuromuscular Disorders +2

Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy

S. Noguchi, Elizabeth M. McNally, Kamel Ben Othmane et al. · Science · 1995 · 510 citations

Medicine, Genetics, Molecular Genetics +15

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

Leland E. Lim, Franck Duclos, Odile Broux et al. · Nature Genetics · 1995 · 449 citations

Medicine, Biochemistry, Molecular Biology +10

β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

Carsten G. Bönnemann, Raju Modi, S. Noguchi et al. · Nature Genetics · 1995 · 446 citations

Medicine, Genetics, Molecular Genetics +10