Determining the mechanism for lung lipid defects in a Mecp2-mutant mouse model for Rett syndrome
Determining the mechanism for lung lipid defects in a Mecp2-mutant mouse model for Rett syndrome
确定 Mecp2 突变小鼠 Rett 综合征模型中肺脂质缺陷的机制
批准号：
383417
负责人：
Vashi Neeti
金额：
$7.65万
依托单位国家：
加拿大
项目类别：
Studentship Programs
财政年份：
2017
资助国家：
加拿大
项目状态：
已结题
起止时间：
2017-10-01 至 2020-10-01
中文摘要
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英文摘要
Rett syndrome (RTT) is a severe neurological disorder that almost exclusively affects females and is caused by mutations in the gene methyl-CpG-binding protein 2 (MECP2). Girls with RTT reach their normal developmental milestones, but soon lose their abil
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