Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family

Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family

Abstract This research resulted in the identification and submission of a novel RUNX2 gene mutation in the affected members of the studied pedigree. Mutation screening is an effective method for the early diagnosis of CCD in the affected individuals.

Bibliographic Details
Main Authors: Omid Daneshjoo, Pirooz Ebrahimi, Leila B. Salehi, Antonio Pizzuti, Masoud Garshasbi
Format: Article
Language:English
Published: Wiley 2020-12-01
Series:Clinical Case Reports
Subjects:
autosomal dominant
cleidocranial dysplasia
RUNX2 gene
sequencing
Online Access:https://doi.org/10.1002/ccr3.2825

Internet

https://doi.org/10.1002/ccr3.2825

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