Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia

Tooth agenesis is one of the most common craniofacial disorders in humans. More than 350 genes have been associated with teeth development. In this study, we enrolled 60 child patients (age 13 to 17) with various types of tooth agenesis. Whole gene sequences of PAX9, MSX1, AXIN2, EDA, EDAR and WNT10...

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Detalles Bibliográficos
Publicado en:PLoS One
Main Authors: Bonczek, Ondřej, Bielik, Peter, Krejčí, Přemysl, Zeman, Tomáš, Izakovičová-Hollá, Lýdie, Šoukalová, Jana, Vaněk, Jiří, Gerguri, Tereza, Balcar, Vladimir J., Šerý, Omar
Formato: Artigo
Idioma:Inglês
Publicado: Public Library of Science 2018
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6128526/
https://ncbi.nlm.nih.gov/pubmed/30192788
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0202989
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