The Effect of an Autism-Associated Polymorphism in the STK39 Gene on the Autism Symptom Domains

被引:0
作者
Rick D. Vavolizza
James Schmeidler
Nicolas Ramoz
Joseph D. Buxbaum
Christopher J. Smith
Jeremy M. Silverman
机构
[1] University of North Carolina,Department of Psychiatry
[2] Mount Sinai School of Medicine,INSERM UMR894
[3] University Paris Descartes,undefined
[4] Southwest Autism Research and Resource Center,undefined
来源
Journal of Autism and Developmental Disorders | 2012年 / 42卷
关键词
Single Nucleotide Polymorphism; Autism Spectrum Disorder; Autism Trait; Pervasive Developmental Disorder; Rs1807984 Single Nucleotide Polymorphism;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:319 / 320
页数:1
相关论文
共 23 条
[1]  
Lord C(1994)Autism diagnostic interview—revised a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders Journal of Autism and Developmental Disorders 24 659-685
[2]  
Rutter M(2008)An analysis of candidate autism loci on chromosome 2q24–q33: Evidence for association to the STK39 gene American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics 147 1152-1158
[3]  
Le Couteur A(2001)Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics 147 408-410
[4]  
Ramoz N(2001)Symptom domains in autism and related conditions: evidence for familiality American Journal of Medical Genetics 114 64-73
[5]  
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