Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protei
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protei is one of 9,000 studies in the ScholarPulse dataset. Key details — Authors: Ruthie E. Amir, Ignatia B. Van den Veyver, Mimi Wan, Charles Q. Tran, Uta Francke, Huda Y. Zoghbi; Journal / source: Nature Genetics; Year: 1999.
| Authors | Ruthie E. Amir, Ignatia B. Van den Veyver, Mimi Wan, Charles Q. Tran, Uta Francke, Huda Y. Zoghbi |
|---|---|
| Journal / source | Nature Genetics |
| Year | 1999 |
| Field | Genetics and Neurodevelopmental Disorders |
| Times cited | 5024 |
| Type | article |
| DOI / link | https://doi.org/10.1038/13810 |