Associated Papers
Critical Considerations in Calling Disease-Causing EDAR Mutations in Nonsyndromic Oligodontia.
Kim YJ et al.
Journal of Clinical Medicine, 2024
Identification of potential key variants in mandibular premolar hypodontia through whole-exome sequencing.
Lee S et al.
Frontiers in Genetics, 2023
Novel LRP6 Mutations Causing Non-Syndromic Oligodontia.
Lee Y et al.
Journal of Personalized Medicine, 2022
A novel EDAR missense mutation identified by whole-exome sequencing with non-syndromic tooth agenesis in a Chinese family.
Zhang H et al.
Molecular Genetics & Genomic Medicine, 2021
Characterisation of a second gain of function EDAR variant, encoding EDAR380R, in East Asia.
Riddell J et al.
European Journal of Human Genetics : Ejhg, 2020
Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR- and EDA-associated nonsyndromic oligodontia.
Zhang L et al.
Human Mutation, 2020
Comprehensive genetic exploration of selective tooth agenesis of mandibular incisors by exome sequencing.
Yamaguchi T et al.
Human Genome Variation, 2017
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