Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency-Reference-Cited by-同舟云学术

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Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency

Published:2008-04 Issue:4 Volume:93 Page:450-457
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Lee Hsien-Hsiung,Lee Yann-Jinn,Wang Yu-Mei,Chao Hsiang-Tai,Niu Dau-Ming,Chao Mei-Chyn,Tsai Fuu-Jen,Lo Fu-Sung,Lin Shio-Jean

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 24 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. Targeted long-read sequencing for comprehensive detection of CYP21A2 mutations in patients with 21-hydroxylase deficiency;Journal of Endocrinological Investigation;2023-10-10

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

3. Genetic analysis and novel variation identification in Chinese patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency;The Journal of Steroid Biochemistry and Molecular Biology;2022-09

4. Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management;Endocrine Reviews;2021-05-07

5. The spectrum of CYP21A2 gene mutations in patients with classic salt wasting form of 2l‐hydroxylase deficiency in a Chinese cohort;Molecular Genetics & Genomic Medicine;2020-09-21

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