Molecular analysis of the CYP21A2 gene in Chinese patients with steroid 21-hydroxylase deficiency-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Molecular analysis of the CYP21A2 gene in Chinese patients with steroid 21-hydroxylase deficiency

Published:2014-04 Issue:6 Volume:47 Page:455-463
ISSN:0009-9120
Container-title:Clinical Biochemistry
language:en
Short-container-title:Clinical Biochemistry

Author:

Ma Dingyuan,Chen Yulin,Sun Yun,Yang Bing,Cheng Jian,Huang Meilian,Zhang Jin,Zhang Jingjing,Hu Ping,Lin Ying,Jiang Tao,Xu Zhengfeng

Funder

Medical Leading Talent and Innovation Team Project of Jiangsu Province

Foundation of Nanjing Science and Technology Bureau

Key Technology R&D Program of Jiangsu Province

Foundation of Nanjing Public Health Department

Foundation of Nanjing Medical University

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference36 articles.

1. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency;White;Endocr Rev,2000

2. The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders;Miller;Endocr Rev,2011

3. Genetics of congenital adrenal hyperplasia;Krone;Best Pract Res Clin Endocrinol Metab,2009

4. Impact of molecular genetics on congenital adrenal hyperplasia management;Balsamo;Sex Dev,2010

5. Comparing the Southern blot method and polymerase chain reaction product analysis for chimeric RCCX detection in CYP21A2 deficiency;Lee;Anal Biochem,2010

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Long-read sequencing: An effective method for genetic analysis of CYP21A2 variation in congenital adrenal hyperplasia;Clinica Chimica Acta;2023-07

2. Long-read Amplicon Sequencing of the CYP21A2 in 48 Thai Patients With Steroid 21-Hydroxylase Deficiency;The Journal of Clinical Endocrinology & Metabolism;2022-04-01

3. Genetic aetiology of primary adrenal insufficiency in Chinese children;BMC Medical Genomics;2021-06-30

4. CYP21A2 mutations in pediatric patients with congenital adrenal hyperplasia in Costa Rica;Molecular Genetics and Metabolism Reports;2021-06

5. Neonatal Screening and Genotype-Phenotype Correlation of 21-Hydroxylase Deficiency in the Chinese Population;Frontiers in Genetics;2021-01-22

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3