Kamel Ben Othmane
Duke University(US)Center for Human Genetics(US)Duke Medical Center(US)Duke University Hospital(US)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Genetic Neurodegenerative Diseases, Muscle Physiology and Disorders, RNA Research and Splicing, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy(1995)507 cited
- → Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21(2001)368 cited
- → Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q(1993)177 cited
- → Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q(1992)175 cited
- → Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity(1993)159 cited
- Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.(1996)
- → Identification of a New Locus for Autosomal Recessive Charcot–Marie–Tooth Disease with Focally Folded Myelin on Chromosome 11p15(1999)