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Article

NR0B1 (DAX1) mutations in patients affected by congenital adrenal hypoplasia with growth hormone deficiency as a new finding.

Journal of applied genetics - 1 May 2013

Rojek Aleksandra, Obara-Moszynska Monika, Malecka Elzbieta, Slomko-Jozwiak Malgorzata, Niedziela Marek

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Share to Adrenal Hyperplasia, Congenital
Share to Adrenal Insufficiency
Share to Child, Preschool
Share to DAX-1 Orphan Nuclear Receptor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Dwarfism, Pituitary

Share to Genetic Diseases, X-Linked

Share to Human Growth Hormone

Share to Mutation

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Identifiers

PMID: 23378245
DOI: 10.1007/s13353-013-0135-3

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NR0B1 (DAX1) mutations in patients affected by congenital adrenal hypoplasia with growth hormone deficiency as a new finding.PMID 23378245Read ↗

Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita.Semantic proximity Read ↗

X-linked Congenital Adrenal Hypoplasia with a Novel NR0B1/DAX Gene Mutation.Semantic proximity Read ↗

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A novel DAX1/NR0B1 mutation in a patient with adrenal hypoplasia congenita and hypogonadotropic hypogonadism.Semantic proximity Read ↗

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A Case of X-Linked Adrenal Hypoplasia Congenital (AHC) Due to Large Deletion of NR0B1 (DAX1) and Contiguous Gene.Semantic proximity Read ↗

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Role of DAX-1 (NR0B1) and steroidogenic factor-1 (NR5A1) in human adrenal function.Semantic proximity Read ↗

Analysis of DAX1 (NR0B1) and Steroidogenic Factor-1 (NR5A1) in Children and Adults with Primary Adrenal Failure: Ten Years’ ExperienceSemantic proximity Read ↗

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