A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome

Fuente: Wiley Open Access

Saved in:

Bibliographic Details
Main Authors:	Maryam Arefzadeh, Bahareh Rabbani, Saeideh Abdolahpour, Farnoosh Emami, Farzaneh Abbasi, Tannaz Masoumi, Siamak Mirab Samiee, Ali Rabbani, Nejat Mahdieh
Format:	Artículo Open Access
Published:	Wiley 2026
Subjects:	Clinical Case Reports
Online Access:	Acceder al recurso
Tags:	Add Tag No Tags, Be the first to tag this record!

Internet