Clinical and genetic analysis of patients with cherubism

ConclusionThree different point mutations in the SH3BP2 gene were detected with variable clinical involvement. Genotype‐phenotype association studies in larger population with cherubism are necessary to provide important knowledge about molecular mechanisms related to the disease.This article is protected by copyright. All rights reserved. (Source: Oral Diseases)

from ! Medicine by Alexandros G. Sfakianakis via alwin on Inoreader http://ift.tt/2sAG24r
via IFTTT