Associated Papers
Delayed Diagnosis of X-Linked Adrenal Hypoplasia Congenita in a Boy with a Novel NR0B1 Variant: A Case Report.
Kim SH et al.
Children (basel, Switzerland), 2025
Isolated hypoaldosteronism as first sign of X-linked adrenal hypoplasia congenita caused by a novel mutation in NR0B1/DAX-1 gene: a case report.
Iughetti L et al.
Bmc Medical Genetics, 2019
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