CrossRef Text and Data Mining
Result of CrossRef Text and Data Mining Search is the related articles with entitled article. If you click link1 or link2 you will be able to reach the full text site of selected articles; however, some links do not show the full text immediately at now. If you click CrossRef Text and Data Mining Download icon, you will be able to get whole list of articles from literature included in CrossRef Text and Data Mining.
Functional Identification of Compound Heterozygous Mutations in the CYP17A1 Gene Resulting in Combined 17α-Hydroxylase/17,20-Lyase Deficiency
Eun Yeong Mo, Ji-young Lee, Su Yeon Kim, Min Ji Kim, Eun Sook Kim, Seungok Lee, Je Ho Han, Sung-dae Moon
Endocrinol Metab. 2018;33(3):413-422.   Published online September 18, 2018
DOI: https://doi.org/10.3803/EnM.2018.33.3.413

Excel Download

Functional Identification of Compound Heterozygous Mutations in the CYP17A1 Gene Resulting in Combined 17α-Hydroxylase/17,20-Lyase Deficiency
Endocrinology and Metabolism. 2018;33(3):413   Crossref logo
Link1 Link2 Link3

A Novel Compound Heterozygous CYP17A1 Variant Causes 17α-Hydroxylase/17, 20-Lyase Deficiency
Frontiers in Genetics. 2019;10:   Crossref logo
Link1

Induction of endometrial cycles and ovulation in a woman with combined 17α-hydroxylase/17,20-lyase deficiency due to compound heterozygous mutations on the P45017α gene
Fertility and Sterility. 2000;73(6):1183-1186   Crossref logo
Link1 Link2

17α-Hydroxylase/17, 20-Lyase Deficiency☆
Reference Module in Biomedical Sciences. 2014;   Crossref logo
Link1 Link2

Novel CYP17A1 mutation in a Japanese patient with combined 17α-hydroxylase/17,20-lyase deficiency
Metabolism. 2010;59(2):275-278   Crossref logo
Link1 Link2

A novel compound heterozygous mutation in the CYP17 (P450 17α-hydroxylase) gene leading to 17α-hydroxylase/17,20-lyase deficiency
Metabolism. 2003;52(4):488-492   Crossref logo
Link1 Link2

Three novel CYP17A1 gene mutations (A82D, R125X, and C442R) found in combined 17α-hydroxylase/17,20-lyase deficiency
Metabolism. 2011;60(10):1386-1391   Crossref logo
Link1 Link2

Combined 17α-hydroxylase/17,20-lyase deficiency caused by heterozygous stop codons in the cytochrome P450 17α-hydroxylase gene
Clinical Endocrinology. 1993;39(4):483-485   Crossref logo
Link1

Molecular basis of apparent isolated 17,20-lyase deficiency: compound heterozygous mutations in the C-terminal region (Arg(496) → Cys, Gln(461) → Stop) actually cause combined 17α-hydroxylase/17,20-lyase deficiency
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1992;1139(4):275-279   Crossref logo
Link1 Link2

Loss of Cytochrome P450 17A1 Protein Expression in a 17α-Hydroxylase/17,20-Lyase-Deficient 46,XY Female Caused by Two Novel Mutations in the CYP17A1 Gene
Endocrine Pathology. 2009;20(4):249-255   Crossref logo
Link1 Link2 Link3