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GENETIC STUDIES OF HUMAN DEVELOPMENT DISORDERS

GENETIC STUDIES OF HUMAN DEVELOPMENT DISORDERS
人类发育障碍的遗传学研究
批准号：
7375105
负责人：
Elena V Semina
金额：
$1.8万
依托单位：
MEDICAL COLLEGE OF WISCONSIN
依托单位国家：
美国
项目类别：
财政年份：
2005
资助国家：
美国
项目状态：
已结题
起止时间：
2005-12-01 至 2006-11-30
来源：
https://reporter.nih.gov/project-details/7375105
关键词：
GENETICSTUDIESHUMANDEVELOPMENTDISORDERS

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中文摘要
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英文摘要
This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The main hypothesis of this project is that inherited forms of anterior segment dysgeneis are caused by a change in the genes responsible for ocular development. Our goals are to identify genes involved in human ocular disorders and to identify mutations which cause anterior segment dysgenesis disorders.
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