Identification of a novel mutation in CYP17A1 gene-Reference-Cited by-同舟云学术

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Identification of a novel mutation in CYP17A1 gene

Published:2013-01 Issue:1 Volume:161 Page:44-49
ISSN:1931-5244
Container-title:Translational Research
language:en
Short-container-title:Translational Research

Author:

Xue Li-Qiong,Han Bing,Chen Li-Bo,Pan Chun-Ming,Zhu Hui,Liu Bing-Li,Liu Wei,Wu Wan-Ling,Chen Ming-Dao,Lu Ying-Li,Qiao Jie,Song Huai-Dong

Publisher

Elsevier BV

Subject

Biochemistry (medical),Public Health, Environmental and Occupational Health,General Medicine,Physiology (medical)

Reference21 articles.

1. Congenital adrenal hyperplasia and P450 oxidoreductase deficiency;Krone;Clin Endocrinol (Oxf),2007

2. Cloning and sequence of the human gene encoding P450c17 (steroid 17_-hydroxylase/17,20 lyase): similarity to the gene for P450c21;Picado-Leonard;DNA,1987

3. Regional mapping of genes encoding human steroidogenic enzymes: P450scc to 15q23-q24, adrenodoxin to 11q22; adrenodoxin reductase to 17q24-q25; and P450c17 to 10q24-q25;Sparkes;DNA Cell Biol,1991

4. Cytochrome P450c17 (steroid 17_-hydroxylase/17,20 lyase): cloning of human adrenal and testis cDNAs indicates the same gene is expressed in both tissues;Chung;Proc Natl Acad Sci U S A,1987

5. Prevalence of common mutations in the CYP17A1 gene in Chinese Han population;Bao;Clin Chim Acta,2011

Cited by 3 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. Phenotypic Heterogeneity and Fertility Potential of Patients With 17-Hydroxylase/17,20-lyase Deficiency;The Journal of Clinical Endocrinology & Metabolism;2022-01-19

2. Comparative analyses of hypothalamus transcriptomes reveal fertility-, growth-, and immune-related genes and signal pathways in different ploidy cyprinid fish;Genomics;2021-03

3. Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report;Journal of Medical Case Reports;2019-07-30

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