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5 articles related to "Cyp17a1 Gene"

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Articles

Original Research

Published on 22 Oct 2019

A Novel Compound Heterozygous CYP17A1 Variant Causes 17α-Hydroxylase/17, 20-Lyase Deficiency

in Genetics of Common and Rare Diseases

Hong Chen
Ke Yuan
Bingtao Zhang
Zexiao Jia
Chun Chen
Yilin Zhu
Yaping Sun
Hui Zhou
Wendong Huang
Li Liang

Frontiers in Genetics

doi 10.3389/fgene.2019.00996

7,465 views
15 citations

Original Research

Published on 11 Jun 2018

A Study on the Association Between Polymorphisms in the Cytochrome P450 Family 17 Subfamily A Member 1 Gene Region and Type 2 Diabetes Mellitus in Han Chinese

in Clinical Diabetes

Long Wang
Yu-Ming Niu
Shi-Shi Wu
Chao Zhang
Li Zhou
Hong-Xia Zuo
Peng Wang

Frontiers in Endocrinology

doi 10.3389/fendo.2018.00323

4,985 views
12 citations

Case Report

Published on 21 Sep 2022

Case report: 17α− hydroxylase deficiency due to a hotspot variant and a novel compound heterozygous variant in the CYP17A1 gene of five Chinese patients

in Pediatric Endocrinology

Jinying Li
Qiang Zhang
Jing Chen
Xingjiao Fu
Jingpin Yang
Lijun Liu

Frontiers in Pediatrics

doi 10.3389/fped.2022.935191

3,336 views
4 citations

Case Report

Published on 19 Oct 2022

An Asian case of combined 17α-hydroxylase/17,20-lyase deficiency due to homozygous p.R96Q mutation: A case report and review of the literature

in Pediatric Endocrinology

Qian Liao
Rufei Shen
Mingyu Liao
Chenxi Ran
Ling Zhou
Yuling Zhang
Guiliang Peng
Zheng Sun
Hongting Zheng
Min Long

Frontiers in Endocrinology

doi 10.3389/fendo.2022.989447

4,851 views
1 citation

Case Report

Published on 15 Dec 2022

Ovarian gonadoblastoma with dysgerminoma in a girl with 46,XX karyotype 17a-hydroxylase/17, 20-lyase deficiency: A case report and literature review

in Pediatric Endocrinology

Min Yin
Jiaxin Yang
Qinjie Tian
Xinyue Zhang

Frontiers in Endocrinology

doi 10.3389/fendo.2022.989695

5,539 views
4 citations