Associated Papers
Inhibition of NR5A1 Phosphorylation Alleviates a Transcriptional Suppression Defect Caused by a Novel NR0B1 Mutation.
Abe I et al.
Journal of the Endocrine Society, 2022
X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism: Identification and in vitro study of a novel small indel in the NR0B1 gene.
Yu T et al.
Molecular Medicine Reports, 2016
Three cases of congenital adrenal hypoplasia with novel mutations in the (NROB1) DAX-1 gene.
Wheeler B et al.
Annals of Clinical Biochemistry, 2008
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