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1. Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11.

Author

De Sandre-Giovannoli A, Delague V, Hamadouche T, Chaouch M, Krahn M, Boccaccio I, Maisonobe T, Chouery E, Jabbour R, Atweh S, Grid D, Mégarbané A, and Lévy N

Subjects
Adult, Algeria ethnology, Charcot-Marie-Tooth Disease ethnology, Charcot-Marie-Tooth Disease pathology, Chromosome Mapping, Demyelinating Diseases ethnology, Demyelinating Diseases pathology, Female, Genes, Recessive, Genetic Testing, Humans, Lebanon ethnology, Male, Pedigree, Sural Nerve pathology, Charcot-Marie-Tooth Disease genetics, Chromosomes, Human, Pair 12 genetics, Chromosomes, Human, Pair 13 genetics, Demyelinating Diseases genetics, Homozygote
Published
2005
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