| 项目编号 |
PRJCA024342 |
| 项目标题 |
MAPT mutation |
| 涉及领域 |
Medical |
| 数据类型 |
Raw sequence reads
|
| 物种名称 |
Homo sapiens
|
| 描述信息 |
A Novel G342L MAPT mutation in familial Progressive Supranuclear Palsy Syndrome |
| 样品范围 |
Monoisolate |
| 发布日期 |
2024-03-15 |
| 出版信息 |
| PubMed ID |
文章标题 |
杂志名称 |
Doi |
发表年份 |
| 38708005
|
A novel MAPT variant (E342K) as a cause of familial progressive supranuclear palsy
|
Frontiers in Neurology
|
10.3389/fneur.2024.1372507
|
2024
|
|
|
| 项目资金来源 |
| 机构 |
项目类型 |
授权项目ID |
授权项目名称 |
| the National High Level Hospital Clinical Research Funding
|
|
2022-PUMCH-B-070
|
|
|
|
| 提交者 |
yanfeng
Li (2279519105@qq.com)
|
| 提交单位 |
Peking Union Medical College Hospital |
| 提交日期 |
2024-03-15 |
