Identification of a Novel Mutation in an Iranian Family With 17-β Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Series
Crossref DOI link: https://doi.org/10.32598/JPR.10.1.960.2
Published Online: 2022-01-01
Update policy: https://doi.org/10.32598/NSP.CROSSMARK-POLICY
Heidari, Abolfazl
,
Homaei, Ali
Saffari, Fatemeh
