Institut National de Neurologie Mongi-ben Hamida

Top Publications

Top Publications Authored or Co-Authored in "Institut National de Neurologie Mongi-ben Hamida"

• VPS35 mutations in parkinson disease

  American Journal of Human Genetics, Volume 89, No. 1, Year 2011, Citations 828
• The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

  Nature Genetics, Volume 29, No. 2, Year 2001, Citations 761
• Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein

  Nature Genetics, Volume 9, No. 2, Year 1995, Citations 520
• Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy

  Science, Volume 270, No. 5237, Year 1995, Citations 486
• The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

  Nature Genetics, Volume 26, No. 3, Year 2000, Citations 391