Linkage mapping of a new syndromic form of X-linked mental retardation, MRXS7, associated with obesity

被引:13
作者
Ahmad, W
De Fusco, M
ul Haque, MF
Aridon, P
Sarno, T
Sohail, M
ul Haque, S
Ahmad, M
Ballabio, A
Franco, B
Casari, G
机构
[1] Telethon Inst Genet & Med, I-20132 Milan, Italy
[2] Northwestern Univ, Sch Med, Dept Neurol Cell & Mol Biol, Chicago, IL USA
[3] Univ Oxford, Dept Biochem, Oxford OX1 2JD, England
[4] Quaid I Azam Univ, Dept Biol Sci, Islamabad, Pakistan
[5] Univ Vita Salute, Milan, Italy
关键词
X-linked mental retardation; obesity; linkage mapping;
D O I
10.1038/sj.ejhg.5200376
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A new syndromic form of X-linked mental retardation associated to obesity, MRXS7, has been localised to Xp11.3-Xq23 in a large Pakistani family. The ten affected males show clinical manifestations of mental retardation, obesity and hypogonadism. The family was genotyped by a set of microsatellite markers spaced at approximately 10 cM intervals on the X chromosome. Linkage to five adjacent microsatellite markers, mapping in the pericentromeric area, was established and a maximum two-point lod score of 3.86 was reached at zero recombination with marker DXS1106. Reduced recombination events around the centromere prevented precise mapping of the gene.
引用
收藏
页码:828 / 832
页数:5
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