Identification of potential key variants in mandibular premolar hypodontia through whole-exome sequencing

Determining genotype–phenotype correlations in patients with hypodontia is important for understanding disease pathogenesis, although only a few studies have elucidated it. We aimed to identify genetic variants linked to non-syndromic bilateral mandibular second premolar hypodontia in a Korean popul...

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Detalles Bibliográficos
Autores principales: Lee, Shinyeop, Ahn, Hyunsoo, Kim, Hyeonhye, Lee, Kwanghwan, Kim, Sanguk, Lee, Jae Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514915/
https://www.ncbi.nlm.nih.gov/pubmed/37745851
http://dx.doi.org/10.3389/fgene.2023.1248326

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514915/
https://www.ncbi.nlm.nih.gov/pubmed/37745851
http://dx.doi.org/10.3389/fgene.2023.1248326

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