Mongi Ben Hamida

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Jing Liu, Masashi Aoki, Isabel Illa et al. · Nature Genetics · 1998 · 919 citations

Medicine, Genetics, Molecular Genetics +12

Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein

Karim Ouahchi, Makoto Arita, Herbert J. Kayden et al. · Nature Genetics · 1995 · 571 citations · Full text

Life Sciences, Genetics, Neurology +11

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

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21

Rachel V. Baxter, Kamel Ben Othmane, Julie M. Rochelle et al. · Nature Genetics · 2001 · 369 citations

Life Sciences, Genetics, Neuroscience +10

Severe childhood muscular dystrophy affecting both sexes and frequent in tunisia

Mongi Ben Hamida, Michel Fardeau · Muscle & Nerve · 1983 · 179 citations

Medicine, Pathology, Pediatrics +13