The HOXA1 A218G polymorphism and autism:: Lack of association in white and black patients from the South Carolina Autism Project

被引:11
作者
Collins, JS [1 ]
Schroer, RJ [1 ]
Bird, J [1 ]
Michaelis, RC [1 ]
机构
[1] Greenwood Genet Ctr, JC Self Res Inst, Greenwood, SC 29646 USA
关键词
neurobehavioral disorders; single nucleotide polymorphism; homeobox genes;
D O I
10.1023/A:1024414803151
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
A recent study has suggested that the A218G polymorphism in the homeobox A1 (HOXA1) gene may influence susceptibility to autism. We have determined the frequencies of the A and G alleles of the HOXA1 A218G polymorphism in both white and black patients from the South Carolina Autism Project ( SCAP) and controls. Marked differences were found in allele frequencies between the races, but no deviations from Hardy-Weinberg equilibrium were seen in either white or black SCAP family members. More direct tests, comparing genotype frequencies between probands and controls and tracking transmission of the A versus G alleles to affected offspring, did not support the contention that allele status for the HOXA1 A218G polymorphism influences one's susceptibility to autism.
引用
收藏
页码:343 / 348
页数:6
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