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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i: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
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2018
Fag:
Research Article
Online adgang: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
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker