K. B. Othmane

发表

Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A.

M. Pericak-Vance, J. Vance, M. Hamida, 1995, Genomics.

The gene encoding ganglioside- induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease

J. Gilbert, M. Pericak-Vance, J. Vance, 2001 .

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21

J. Gilbert, M. Pericak-Vance, J. Vance, 2002, Nature Genetics.

Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.

L. Kunkel, J. Vance, M. Passos-Bueno, 1996, American journal of human genetics.

Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy

L. Kunkel, J. Vance, L. Middleton, 1995, Science.

Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q

M. Pericak-Vance, A. Roses, A. Bowcock, 1992, Nature Genetics.

Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B.

J. Vance, J. Stajich, M. Speer, 1996, American journal of human genetics.

Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.

M. Pericak-Vance, J. Vance, M. Hamida, 1999, Genomics.

Evidence for Linkage Disequilibrium in Chromosome 1 3-Linked

K. B. Othmane, Chritiane Ben Hamida, 2007 .

Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity.

M. Pericak-Vance, A. Roses, J. Vance, 1993, Genomics.