Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.

Author:

Harada F.,Kimura A.,Iwanaga T.,Shimozawa K.,Yata J.,Sasazuki T.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Cited by 79 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. A MinION-based Long-Read Sequencing Application With One-Step PCR for the Genetic Diagnosis of 21-Hydroxylase Deficiency;The Journal of Clinical Endocrinology & Metabolism;2023-10-06

2. Prenatal Diagnosis and Treatment in Congenital Adrenal Hyperplasia;Fertility and Reproductive Outcomes in Different Forms of Congenital Adrenal Hyperplasia;2021

3. Defects of Adrenal Steroidogenesis;Endocrinology: Adult and Pediatric;2016

4. A de novo mutation in CYP21A2 gene in a case of in vitro fertilization;Molecular Genetics and Metabolism Reports;2015-12

5. Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche;European Journal of Endocrinology;2011-08

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