Refined mapping of the HMSNR critical gene region-construction of a high-density integrated genetic and physical map

被引:12
作者
Hantke, J
Rogers, T
French, L
Tournev, I
Guergueltcheva, V
Urtizberea, JA
Colomer, J
Corches, A
Lupu, C
Merlini, L
Thomas, PK
Kalaydjieva, L [1 ]
机构
[1] Univ Western Australia, Western Australian Inst Med Res, Perth, WA 6009, Australia
[2] Univ Western Australia, Med Res Ctr, Perth, WA 6009, Australia
[3] Wellcome Trust Sanger Inst, Cambridge, England
[4] Med Univ, Dept Neurol, Sofia, Bulgaria
[5] Ethn Minor Hlth Problems Fdn, Sofia, Bulgaria
[6] Hop Raymond Poincare, Serv MPR Enfant, Garches, France
[7] Hosp St Joan de Deu, Barcelona, Spain
[8] Cent Clin Neuropsihiatrie Pentru Copii Adolescent, Timisoara, Romania
[9] Ist Ortoped Rizzoli, Bologna, Italy
[10] Inst Neurol, London WC1N 3BG, England
[11] UCL Natl Hosp Neurol & Neurosurg, London WC1N 3BG, England
关键词
ARCMT; Charcot-Marie-Tooth disease; hereditary motor and sensory neuropathy Russe refined mapping;
D O I
10.1016/S0960-8966(03)00098-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Hereditary motor and sensory neuropathy russe, a form of autosomal recessive Charcot-Marie-Tooth disease, is a rare disorder found in several Roma families front Europe. The gene has been mapped to a 1 Mb region on 10q22. Detailed analysis led to the exclusion of 22 candidate genes and the assembly of a high-density genetic map comprising 141 polymorphic markers. Extensive genotyping in an extended sample of affected families resulted in a 10-fold reduction of the critical hereditary motor and sensory neuropathy russe gene region, which is now contained within a single completely sequenced BAC clone. The fact that no sequence variant has been detected in the known genes in the critical region indicates that the hereditary motor and sensory neuropathy russe mutation affects a novel gene that remains to be identified. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:729 / 736
页数:8
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