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Fine localization of the CMT4A locus using a PAC contig and haplotype analysis
Authors:Kamel Ben Othmane  Julie M. Rochelle  Mongi Ben Hamida  Brandon Slotterbeck  Nagesh Rao  Faycal Hentati  Margaret A. Pericak-Vance  J. M. Vance
Affiliation:(1) Division of Neurology, Department of Medicine, Duke University Medical Center, Durham, NC 27710-2903, USA, US;(2) Institut National de Neurologie, La Rabta, Tunis, Tunisia,;(3) Department of Pathology and Laboratory Medicine, University of California at Los Angeles School of Medicine, Los Angeles, California, USA, US
Abstract:Charcot-Marie-Tooth disease type 4A (CMT4A) is a severe, autosomal recessive peripheral neuropathy linked to chromosome 8q13-q21. We have previously constructed a YAC contig across the CMT4A region and narrowed the disease-flanking interval to approximately three megabases. Subsequently, we constructed a PAC/BAC contig made of 44 clones and mapped 44 new and 30 previous STSs, ESTs, and polymorphic makers to the region. Using 13 polymorphic markers, we have now identified an ancestral haplotype segregating in three families, indicating a common founder mutation. Two ancestral recombination events in this haplotype significantly reduce the minimal candidate region to a minimal trailing path of five PAC/BAC clones, which will now allow direct investigation of candidate genes for CMT4A. Received: April 8, 1998 / Accepted: June 15, 1998 / Published online: October 28, 1998
Keywords:  Charcot-Marie-Tooth  CMT4A  Haplotype analysis  PAC contigs
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