A novel NR0B1 mutation correlated with X-linked adrenal hypoplasia congenital (AHC)-Reference-Cited by-同舟云学术

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A novel NR0B1 mutation correlated with X-linked adrenal hypoplasia congenital (AHC)

Published:2022-06 Issue: Volume:27 Page:101598
ISSN:2452-0144
Container-title:Gene Reports
language:en
Short-container-title:Gene Reports

Author:

Komachali Sajad Rafiee,Nouri Negar,Zaker Erfan,Mousavi Seyyed Reza,Salehi Mansoor

Funder

NODAI Genome Research Center, Tokyo University of Agriculture

Isfahan University of Medical Sciences

Publisher

Elsevier BV

Subject

Genetics

Reference30 articles.

1. A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans;Achermann;Nat. Genet.,1999

2. X-linked adrenal hypoplasia congenita and DAX-1;Achermann;Endocrinologist,2000

3. A novel single base deletion at codon 434 (1301delT) of the DAX1 gene associated with prepubertal testis enlargement;Argente;Mol. Genet. Metab.,2003

4. Adrenal hypoplasia congenita with phenotypic features suggestive of neurofibromatosis type 1 among three african-american brothers;Balikcioglu;Am. J. Med. Genet. A,2013

5. Congenital adrenal hypoplasia and selective absence of pituitary luteinizing hormone: a new autosomal recessive syndrome;Burke;Am. J. Med. Genet.,1988

Cited by 1 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. A narrative review: an update on primary adrenal insufficiency (PAI) in pediatric population;Pediatric Medicine;2022-01

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