ZFHX3转录因子基因调控房颤机理研究
序号 | 标题 | 类型 | 作者 |
---|---|---|---|
1 | A novel STS mutation and an Xp22.31 microdeletion in a Chinese family with X-linked ichthyosis | 期刊论文 | Yufeng Huang;Sukun Luo;Peiwei Zhao;Li Tan;Guili Fu;Aifen Zhou;Xuelian He |
2 | A 9-month-old Chinese patient with Gabriele-de Vries syndrome due to novel germline mutation in the YY1 gene. | 期刊论文 | Tan Li;Li Ying;Liu Fan;Huang Yufeng;Luo Sukun;Zhao Peiwei;Gu Weiyue;Lin Jun;Zhou Aifen;He Xuelian |
3 | Functional Analysis of a Novel CLN5 Mutation Identified in a Patient With Neuronal Ceroid Lipofuscinosis. | 期刊论文 | Luo Sukun;Bi Bo;Zhu Baiqi;Tan Li;Zhao Peiwei;Huang Yufeng;Wu Gefei;Zhou Aifeng;He Xuelian |