View in EDS HTML Full Text PDF Full Text

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

Saved in:
Bibliographic Details
Title: A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome.
Authors: Arefzadeh, Maryam1 (AUTHOR), Rabbani, Bahareh2 (AUTHOR), Abdolahpour, Saeideh2 (AUTHOR), Emami, Farnoosh2 (AUTHOR), Abbasi, Farzaneh2 (AUTHOR), Masoumi, Tannaz1 (AUTHOR), Mirab Samiee, Siamak3 (AUTHOR), Rabbani, Ali2 (AUTHOR), Mahdieh, Nejat3 (AUTHOR) nmahdieh@yahoo.com
Source: Clinical Case Reports. Mar2026, Vol. 14 Issue 3, p1-5. 5p.
Database: Academic Search Ultimate
Full text is not displayed to guests.
Description
ISSN:20500904
DOI:10.1002/ccr3.72218