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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
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 |
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