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