The First Report of a Missense Variant in RFX2 Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani Family

Background: The syndromic and non-syndromic congenital missing teeth phenotype is termed tooth agenesis. Since tooth agenesis is a heterogeneous disorder hence, the patients show diverse absent teeth phenotypes. Thus identifying novel genes involved in the morphogenesis of ectodermal appendages, inc...

Descripción completa

Detalles Bibliográficos
Autores principales: Khan, Sher Alam, Khan, Saadullah, Muhammad, Noor, Rehman, Zia Ur, Khan, Muhammad Adnan, Nasir, Abdul, Kalsoom, Umm-e-, Khan, Anwar Kamal, Khan, Hassan, Wasif, Naveed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822170/
https://www.ncbi.nlm.nih.gov/pubmed/35145545
http://dx.doi.org/10.3389/fgene.2021.782653

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822170/
https://www.ncbi.nlm.nih.gov/pubmed/35145545
http://dx.doi.org/10.3389/fgene.2021.782653

Ejemplares similares