Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22.

Charcot-Marie-Tooth disease type 4B (CMT4B) is a demyelinating autosomal recessive motor and sensory neuropathy characterized by focally folded myelin sheaths in the peripheral nerve. We recently mapped the CMT4B gene to a 5-cM interval on chromosome 11q22, using homozygosity mapping and haplotype s...

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Bibliographic Details
Main Authors: Bolino, A, Levy, E, Muglia, M, Conforti, F, LeGuern, E, Salih, M, Georgiou, D, Christodoulou, R, Hausmanowa-Petrusewicz, I, Mandich, P, Gambardella, A, Quattrone, A, Devoto, M, Monaco, A
Format: Journal article
Language:English
Published: 2000