| 标题 |
Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression |
| 网址 | |
| DOI | |
| 其它 |
期刊:Human Mutation 作者:Markus Zweier; Anne Gregor; Christiane Zweier; Hartmut Engels; Heinrich Sticht; et al 出版日期:2010-04-06 |
| 求助人 | |
| 下载 |
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(2025-6-4)