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Mutation Analysis of the CYP21A2 Gene in the Iranian Population
Background: Defects in the CYP21A2 gene cause steroid 21-hydroxylase deficiency, which is the most frequent cause of congenital adrenal hyperplasia. Forty four affected families were investigated to identify the mutation spectrum of the CYP21A2 gene. Methods: Families were subjected to clinical, bio...
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| 主要な著者: | , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Mary Ann Liebert, Inc.
2012
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3277924/ https://ncbi.nlm.nih.gov/pubmed/22017335 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2011.0099 |
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