← Evidence map

ArticleAnnals of pediatric endocrinology & metabolism2024

A novel variant in NR0B1 causing X-linked adrenal hypoplasia congenita.

Seung Heo et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

Not cited yet

Full record →Abstract, authors, funding and every citing paper · PMID 38956756