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Mongi Ben Hamida
Researcher Next ID · RN-015210
Researcher · Neuroscience
Institut National de Santé Publique
, Tunisia
Not currently recruitingFunding unknown
- Works count
- 30
- Citation count
- 4,085
- H-index
- 21
- i10-index
- 26
Research interests
Neuroscience
Biochemistry, Genetics and Molecular Biology
Medicine
Neurological diseases and metabolism
Hereditary Neurological Disorders
Muscle Physiology and Disorders
Neurogenetic and Muscular Disorders Research
Amyotrophic Lateral Sclerosis Research
Publications
Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21
Nature Genetics · 2001 · 10.1038/ng796
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
Nature Genetics · 1998 · 10.1038/1682
Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein
Nature Genetics · 1995 · 10.1038/ng0295-141
Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy
Science · 1995 · 10.1126/science.270.5237.819
Current projects
No projects listed.