← Evidence map

ArticleFrontiers in medicine2026

Atypical endocrine manifestations in Gordon syndrome caused by CUL3 mutation: a case report.

Mahsa Fatahichegeni 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 42548885