Ben-Hamida, Mongi G.M.

Top Publications

Top Publications Authored or Co-Authored by "Ben-Hamida, Mongi G.M."

• 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
• Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

  Neurogenetics, Volume 2, No. 1, Year 1998, Citations 197
• Severe childhood muscular dystrophy affecting both sexes and frequent in tunisia

  Muscle & Nerve, Volume 6, No. 7, Year 1983, Citations 171
• Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

  Neurology, Volume 45, No. 4, Year 1995, Citations 155
• Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families

  Neurology, Volume 43, No. 11, Year 1993, Citations 131