NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

被引:86
作者
Gauthier, J
Bonnel, A
St-Onge, J
Karemera, L
Laurent, S
Mottron, L
Fombonne, T
Joober, R
Rouleau, GA
机构
[1] McGill Univ, Inst Res, Hlth Ctr TI MUHC, Montreal, PQ H3G 1A4, Canada
[2] McGill Univ, Douglas Hosp, Res Ctr, Verdun, PQ H4H 1R3, Canada
[3] Hop Riviere Praires, Clin Specialisee Troubles Envahissants Dev, Montreal, PQ, Canada
[4] McGill Univ, Dept Psychiat, Montreal Childrens Hosp, Montreal, PQ, Canada
关键词
neuroligin; autism; X-chromosome;
D O I
10.1002/ajmg.b.30066
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Jamain [2003: Nat Genet 34:27-29] recently reported mutations in two neuroligin genes in sib-pairs affected with autism. In order to confirm these causative mutations in our autistic population and to determine their frequency we screened 96 individuals affected with autism. We found no mutations in these X-linked genes. These results indicate that mutations in NLGN3 and NLGN4 genes are responsible for at most a small fraction of autism cases and additional screenings in other autistic populations are needed to better determine the frequency with which mutations in NLGN3 and NLGN4 occur in autism. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:74 / 75
页数:2
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