[Analysis of CYP21A2 gene mutations in two families with 21-hydroxylase deficiency]. | Zhonghua Yi Xue Yi Chuan Xue Za Zhi;31(3): 289-93, 2014 Jun. | MEDLINE

Main content 1 Search 2 Footer 3

+A A -A High contrast

VHL Regional Portal

Information and Knowledge for Health

Advanced Search EVID@Easy

[Analysis of CYP21A2 gene mutations in two families with 21-hydroxylase deficiency].

Zheng, Ruizhi; Zhao, Zhigang; Wang, Yanfang; Yuan, Huijuan; Wang, Suijun; Su, Yong; Ma, Yuehua; Hu, Zhijing; Tian, Rui; Wang, Limin.

Affiliation

Zheng R; Department of Endocrinology, Henan Provincial Peoples Hospital, Zhengzhou, Henan 450003, P.R. China. Email: zhaozhigang1957@126.com.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 31(3): 289-93, 2014 Jun.

Article in Zh | MEDLINE | ID: mdl-24928004

Subject(s)

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Steroid 21-Hydroxylase / Adrenal Hyperplasia, Congenital / Mutation, Missense Limits: Adult / Child / Female / Humans / Male Language: Zh Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Journal subject: GENETICA MEDICA Year: 2014 Document type: Article Country of publication: China

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Steroid 21-Hydroxylase / Adrenal Hyperplasia, Congenital / Mutation, Missense Limits: Adult / Child / Female / Humans / Male Language: Zh Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Journal subject: GENETICA MEDICA Year: 2014 Document type: Article Country of publication: China