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PTCHD1 in autism and cognition: from function to phenotype

PTCHD1 in autism and cognition: from function to phenotype
PTCHD1 在自闭症和认知中的作用：从功能到表型
批准号：
369372
负责人：
Vincent John B
金额：
$73.29万
依托单位：
Centre for Addiction and Mental Health (Toronto)
依托单位国家：
加拿大
项目类别：
Operating Grants
财政年份：
2017
资助国家：
加拿大
项目状态：
已结题
起止时间：
2017-09-01 至 2022-09-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=369372&lang=en
关键词：
Animal Models Autism Clinical Diagnostic Intellectual Disability Phenotype Protein Function Therapeutic

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中文摘要
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英文摘要
Truncating mutations in the X-linked gene PTCHD1 have been shown to cause autism spectrum disorder (ASD) and/or intellectual disability (ID). While the link between gene and disease is very strong, our understanding of what PTCHD1 does is very weak. Initi
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