CORC  > 中国医学科学院 北京协和医学院
Analysis of novel heterozygous mutations in the CYP11B2 gene causing congenital aldosterone synthase deficiency and literature review
Miao Hui; Yu Zhongxun; Lu Lin; Zhu Huijuan; Auchus Richard J; Liu Jiayan; Jiang Jun; Pan Hui; Gong Fengying; Chen Shi
2019
卷号150页码:108448
关键词Aldosterone synthesis CYP11B2 mutations Hypoaldosteronism Next-generation sequencing
ISSN号1878-5867
DOI10.1016/j.steroids.2019.108448
URL标识查看原文
收录类别PUBMED
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/6338709
专题中国医学科学院 北京协和医学院
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GB/T 7714
Miao Hui,Yu Zhongxun,Lu Lin,et al. Analysis of novel heterozygous mutations in the CYP11B2 gene causing congenital aldosterone synthase deficiency and literature review[J],2019,150:108448.
APA Miao Hui.,Yu Zhongxun.,Lu Lin.,Zhu Huijuan.,Auchus Richard J.,...&Lu Zhaolin.(2019).Analysis of novel heterozygous mutations in the CYP11B2 gene causing congenital aldosterone synthase deficiency and literature review.,150,108448.
MLA Miao Hui,et al."Analysis of novel heterozygous mutations in the CYP11B2 gene causing congenital aldosterone synthase deficiency and literature review".150(2019):108448.
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