Загрузка...
MECP2 missense mutations outside the canonical MBD and TRD domains in males with intellectual disability
Methyl-CpG binding protein 2 (MeCP2) is a nuclear protein highly expressed in neurons that is involved in transcriptional modulation and chromatin remodeling. Mutations in MECP2 in females are associated with Rett syndrome, a neurological disorder characterized by a normal neonatal period, followed...
Сохранить в:
| Опубликовано в: : | J Hum Genet |
|---|---|
| Главные авторы: | , , , , , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2015
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4770571/ https://ncbi.nlm.nih.gov/pubmed/26490184 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jhg.2015.118 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|