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Molecular genetic analysis of CYP21A2 gene in patients with congenital adrenal hyperplasia
CONTEXT: Congenital adrenal hyperplasia (CAH) is one of the inborn errors of metabolic disorder inherited in an autosomal recessive manner caused by the defects in the steroid 21 hydroxylase CYP21A2 gene. We analyzed the genotype of 62 patients with classic CAH. AIMS: To find out the underlying muta...
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| Asıl Yazarlar: | , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Medknow Publications & Media Pvt Ltd
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3354845/ https://ncbi.nlm.nih.gov/pubmed/22629504 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2230-8210.95679 |
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