Identification of mutations in Iranian patients’ DAX-1 gene with X-linked adrenal hypoplasia congenital-Reference-Cited by-同舟云学术

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Identification of mutations in Iranian patients’ DAX-1 gene with X-linked adrenal hypoplasia congenital

Published:2017-04 Issue:2 Volume:18 Page:165-172
ISSN:1110-8630
Container-title:Egyptian Journal of Medical Human Genetics
language:en
Short-container-title:Egyptian Journal of Medical Human Genetics

Author:

Davoodnejad Mahdieh,Eshraghi Peyman,vakili Rahim,Hamzehloie Tayebeh

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical)

Reference22 articles.

1. Addison’s disease due to congenitall adrenal hypoplasia of the adrenals in an infant aged 33days;Skil;J Pathol Bacteriol,1948

2. Molecular mechanisms of DAX1 action;Iyer;Mol Genet Metab,2004

3. An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenital;Zanaria;Nature,1994

4. Congenitall adrenal hypoplasia and hypogonadotropic hypogonadism;Golden;Am J Dis Child,1977

5. Congenitall adrenal hypoplasia and isolated gonadotropin deficiency;Kletter;Trends Endocrinol Metab,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. EWS/FLI1 Characterization, Activation, Repression, Target Genes and Therapeutic Opportunities in Ewing Sarcoma;International Journal of Molecular Sciences;2023-10-14

2. A novel mutation in the DAX1 gene in a newborn with adrenal hypoplasia congenita in Korea;Journal of Genetic Medicine;2017-06-30

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