C. Barhoumi

Linkage of a new locus for autosomal recessive axonal form of Charcot–Marie–Tooth disease to chromosome 8q21.3

C. Barhoumi, Rim Amouri, Christiane Ben Hamida et al. · Neuromuscular Disorders · 2001 · 53 citations

Mendelian Disorder, Cytogenetics, Genetic Disorder +8

Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1

C. Ben Hamida, L Cavalier, Samir Belal et al. · Neurogenetics · 1997 · 52 citations

Molecular Neuroscience, Neurogenomics, Mendelian Disorder +12

Aprataxin gene mutations in Tunisian families

Rim Amouri, Maria-Ceù Moreira, M. Zouari et al. · Neurology · 2004 · 45 citations

Biology, Mendelian Disorder, Genetic Disorder +13

Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness

O. Dubourg, C. Barhoumi, Hamid Azzedine et al. · Muscle & Nerve · 2000 · 22 citations

The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease.

Farid Meggouh, Ali Benomar, H Rouger et al. · Journal of Medical Genetics · 1998 · 22 citations · Full text

Connexin 32, Hereditary Motor, Mendelian Disorder +12