POSSIBLE ASSOCIATION OF THE EXTENDED MHC HAPLOTYPE-B44-SC30-DR4 WITH AUTISM

被引:70
作者
WARREN, RP
SINGH, VK
COLE, P
ODELL, JD
PINGREE, CB
WARREN, WL
DEWITT, CW
MCCULLOUGH, M
机构
[1] UTAH STATE UNIV,DEPT BIOL,LOGAN,UT 84322
[2] UTAH STATE UNIV,DEPT PSYCHOL,LOGAN,UT 84322
[3] UNIV UTAH,DEPT PATHOL,SALT LAKE CITY,UT 84112
关键词
D O I
10.1007/BF00215048
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We previously reported that the complement C4B null allele appears to be associated with infantile autism. Since the C4B null allele is known to be part of the extended or ancestral haplotype [B44-SC30-DR4], we investigated the incidence of [B44-SC30-DR4] in 21 autistic children and their parents. This extended haplotype was increased by almost six-fold in the autistic subjects as compared with healthy controls. Moreover, the total number of extended haplotypes expressed on chromosomes of autistic subjects was significantly increased as compared with those expressed on chromosomes of healthy subjects. We conclude that a gene related to, or included in, the extended major histocompatibility complex may be associated with autism.
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页码:203 / 207
页数:5
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