Загрузка...
Prevalence of CYP17A1 gene mutations in 17α-hydroxylase deficiency in the Chinese Han population
BACKGROUND: 17α-hydroxylase deficiency is a rare autosomal recessive disorder caused by mutations in the cytochrome P450 family 17 subfamily A member 1 gene. The major clinical presentation includes hypertension, hypokalemia, male pseudohermaphroditism and female gonadal dysplasia. Hundreds of patho...
Сохранить в:
| Опубликовано в: : | Clin Hypertens |
|---|---|
| Главные авторы: | , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2019
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6792268/ https://ncbi.nlm.nih.gov/pubmed/31636948 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40885-019-0128-6 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|