載入...
Mutation detection of CYP21A2 gene in nonclassical congenital adrenal hyperplasia patients with premature pubarche
BACKGROUND: Congenital adrenal hyperplasia (CAH) due to mutations in the gene encoding 21-hydroxilase is one of common disease with an autosomal recessive form. In this study, our aim is to detect the prevalence of eight common mutations in nonclassical congenital adrenal hyperplasia (NCAH). MATERIA...
Na minha lista:
| 發表在: | Adv Biomed Res |
|---|---|
| Main Authors: | , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Medknow Publications & Media Pvt Ltd
2016
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4815525/ https://ncbi.nlm.nih.gov/pubmed/27099846 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2277-9175.178794 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|