Загрузка...
MeCP2_e2 partially compensates for lack of MeCP2_e1: A male case of Rett syndrome
Abstract Background Rett syndrome (RTT) is a neurodevelopmental disorder that predominantly affects girls. Its causative gene is the X‐linked MECP2 encoding the methyl‐CpG‐binding protein 2 (MeCP2). The gene comprises four exons and generates two isoforms, namely MECP2_e1 and MECP2_e2. However, it r...
Сохранить в:
| Главные авторы: | , , , , , , , , |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Wiley
2020-02-01
|
| Серии: | Molecular Genetics & Genomic Medicine |
| Предметы: | |
| Online-ссылка: | https://doi.org/10.1002/mgg3.1088 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|