Hammadouche, Tarik

Top Publications

Top Publications Authored or Co-Authored by "Hammadouche, Tarik"

• Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse

  American Journal of Human Genetics, Volume 70, No. 3, Year 2002, Citations 565
• Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma

  American Journal of Human Genetics, Volume 72, No. 5, Year 2003, Citations 278
• The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C gene

  Neuromuscular Disorders, Volume 13, No. 1, Year 2003, Citations 92
• Genetic heterogeneity in giant axonal neuropathy: An Algerian family not linked to chromosome 16q24.1

  Neuromuscular Disorders, Volume 12, No. 9, Year 2002, Citations 22
• The autosomal recessive form of CMT disease linked to 5q31-q33

  Annals of the New York Academy of Sciences, Volume 883, Year 1999, Citations 8