Загрузка...
Diurnal variation in autonomic regulation among patients with genotyped Rett syndrome
BACKGROUND: Rett syndrome is a severe neurological disorder with a range of disabling autonomic and respiratory symptoms and resulting predominantly from variants in the methyl-CpG binding protein 2 gene on the long arm of the X-chromosome. As basic research begins to suggest potential treatments, s...
Сохранить в:
| Опубликовано в: : | J Med Genet |
|---|---|
| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2020
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7891682/ https://ncbi.nlm.nih.gov/pubmed/32156713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2019-106601 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|