Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.
Genomic DNAs from twelve Japanese patients with steroid 21-hydroxylase [21-OHase; steroid 21-monooxygenase; steroid, hydrogen-donor:oxygen oxidoreductase (21-hydroxylating); EC 1.14.99.10] deficiency were analyzed by Southern blot hybridization. A 3.7-kilobase (kb) Taq I and a 1.7-kb Pvu II restrict...
Kaydedildi:
| Yayımlandı: | Proc Natl Acad Sci U S A |
|---|---|
| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
National Academy of Sciences
1987
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC299484/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3500473/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.84.22.8091 |
| Etiketler: |
Etiket eklenmemiş, İlk siz ekleyin!
|