An Exploration of Mutagenesis in a Family with Cleidocranial Dysplasia without RUNX2 Mutation

Cleidocranial dysplasia (CCD) is an autosomal dominant inheritable skeletal disorder characterized by cranial dysplasia, clavicle hypoplasia, and dental abnormalities. Mutations involving Runt-related transcription factor 2 (RUNX2) are currently the only known molecular etiology for CCD but are not...

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Detalles Bibliográficos
Autores principales: Liu, Dandan, Liu, Yang, Zhang, XianLi, Wang, Yixiang, Zhang, Chenying, Zheng, Shuguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560734/
https://www.ncbi.nlm.nih.gov/pubmed/34737766
http://dx.doi.org/10.3389/fgene.2021.748111

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560734/
https://www.ncbi.nlm.nih.gov/pubmed/34737766
http://dx.doi.org/10.3389/fgene.2021.748111

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