Identifying the First Val281L Mutation Causing Nonclassic Congenital Adrenal Hyperplasia in the Central-East Region of Tunisia-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Identifying the First Val281L Mutation Causing Nonclassic Congenital Adrenal Hyperplasia in the Central-East Region of Tunisia

Published:2024-03-28 Issue: Volume: Page:
ISSN:2168-8184
Container-title:Cureus
language:en
Short-container-title:

Author:

Taieb Ach,Farid Hayfa,Zarrouk Oumayma,Ben Abdessalem Fatma,Layouni Saoussen

Publisher

Springer Science and Business Media LLC

Reference11 articles.

1. Extensive clinical experience: nonclassical 21-hydroxylase deficiency;New MI;J Clin Endocrinol Metab,2006

2. Nonclassic congenital adrenal hyperplasia;Witchel S;Int J Pediatr Endocrinol,2010

3. Clinical and biological phenotypes in late-onset 21-hydroxylase deficiency;Dewailly D;J Clin Endocrinol Metab,1986

4. The presence of the 21-hydroxylase deficiency carrier status in hirsute women: phenotype-genotype correlations;Escobar-Morreale HF;Fertil Steril,1999

5. Mutation analysis of the CYP21A2 gene in the Iranian population;Rabbani B;Genet Test Mol Biomarkers,2012

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