Kamel Ben Othmane

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 · 507 citations

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 · 367 citations

Disease Mechanism, Pathogenesis, Experimental Pathology +7

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q

Kamel Ben Othmane, F. Hentatl, Felicia Lennon et al. · Human Molecular Genetics · 1993 · 177 citations

Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q

Kamel Ben Othmane, Mongi Ben Hamida, Margaret A. Pericak‐Vance et al. · Nature Genetics · 1992 · 175 citations

Chromosome Dynamics, Developmental Biology, Mendelian Disorder +9

Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity

Kamel Ben Othmane, Lefkos Middleton, Lorraine Loprest et al. · Genomics · 1993 · 159 citations

Biology, Mendelian Disorder, Genetic Disorder +11