A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3

被引:14
作者
Aslam, M
Wajid, M
Chahrour, MH
Ansar, M
Haque, S
Pham, TL
Santos, RP
Yan, K
Ahmad, W
Leal, SM
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Quaid I Azam Univ, Dept Biol Sci, Islamabad, Pakistan
关键词
3q13.31-q22.3; DFNB42; nonsyndromic; hearing impairment; Pakistan;
D O I
10.1002/ajmg.a.30508
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A consanguineous family with autosomal recessive nonsyndromic hearing impairment (NSHI) was ascertained in Pakistan and displayed significant evidence of linkage to 3q13.31-q22.3. The novel locus (DFNB42) segregating in this kindred, maps to a 21.6 cM region according to a genetic map constructed using data from both the deCode and Marshfield genetic maps. This region of homozygosity is flanked by markers D3S1278 and D3S2453. A maximum multipoint LOD score of 3.72 was obtained at marker D3S4523. DFNB42 represents the third autosomal recessive NSHI locus to map to chromosome 3. (C) 2005 Wiley-Liss, Inc.
引用
收藏
页码:18 / 22
页数:5
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