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新疆维吾尔族儿童21-羟化酶缺乏症基因型与表型的研究
OBJECTIVE: To investigate gene mutations and the relationship between genotypes and clinical phenotypes in Uygur children with 21-hydroxylase deficiency(21-OHD) in Xinjiang, China. METHODS: A total of 20 Uygur children with 21-OHD who visited the hospital between October 2013 and October 2014 were e...
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| Udgivet i: | Zhongguo Dang Dai Er Ke Za Zhi |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
中国当代儿科杂志编辑部
2016
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7403052/ https://ncbi.nlm.nih.gov/pubmed/26903061 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7499/j.issn.1008-8830.2016.02.009 |
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