ロード中...
Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.
Steroid 21-hydroxylase deficiency is caused by mutations in the CYP21B gene. This gene and a highly homologous pseudogene, CYP21A, alternate with the C4A and C4B genes encoding the fourth component of complement. Classical deficiency alleles are frequently caused by deletions of CYP21B or by gene co...
保存先:
| 出版年: | Proc Natl Acad Sci U S A |
|---|---|
| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
National Academy of Sciences
1988
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC280444/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3260033/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.85.12.4436 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|