Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia.

Zhang, Tingting

Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia. [electronic resource] - Archives of oral biology Apr 2019 - 49-56 p. digital

Publication Type: Journal Article

1879-1506

10.1016/j.archoralbio.2019.02.005 doi


Asian People
Cleidocranial Dysplasia--genetics
Core Binding Factor Alpha 1 Subunit--genetics
Humans
Mutation
Protein Splicing
RNA Splice Sites
Exome Sequencing