A de novo mutation in CYP21A2 gene in a case of in vitro fertilization-Reference-Cited by-同舟云学术

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A de novo mutation in CYP21A2 gene in a case of in vitro fertilization

Published:2015-12 Issue: Volume:5 Page:98-102
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Silva-Grecco Roseane Lopes da,de Paula Michelatto Débora,Lincoln-de-Carvalho Carolina Rodrigues,Henrique Pamela Pontes,da Cunha Heloísa Marcelina,Palandi-de-Mello Maricilda^ORCID

Funder

FAPESP grants

FAPESP Doctoral Fellowship

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference38 articles.

1. 21-Hydroxylase-deficient congenital adrenal hyperplasia;Nimkarn;Gene Reviews®[Internet],2013

2. Steroid 21-hydroxylase deficiency congenital adrenal hyperplasia;Nimkarn;Pediatr. Clin. N. Am.,2011

3. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency;White;Endocr. Rev.,2000

4. Androgen synthesis in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Kamrath;Horm. Metab. Res.,2013

5. Congenital adrenal hyperplasias;Miller;Endocrinol. Metab. Clin. N. Am.,1991

Cited by 2 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. Molecular Diagnosis of Steroid 21-Hydroxylase Deficiency: A Practical Approach;Frontiers in Endocrinology;2022-03-29

2. The molecular basis and genotype–phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population;Molecular Biology Reports;2019-04-20

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