MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin
| Autor: | Trappe, R., Laccone, F., Cobilanschi, J., Meins, M., Huppke, P., Hanefeld, F., Engel, W. |
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| Zdroj: | In The American Journal of Human Genetics 2001 68(5):1093-1101 |
| Databáze: | ScienceDirect |
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