Identification of a Novel FAM83H Mutation and Management of Hypocalcified Amelogenesis Imperfecta in Early Childhood

Amelogenesis imperfecta (AI) is a heterogeneous group of rare genetic disorders affecting amelogenesis during dental development. Therefore, the molecular genetic etiology of AI can provide information about the nature and progress of the disease. To confirm the genetic etiology of AI in a Korean fa...

Descripción completa

Detalles Bibliográficos
Autores principales: Song, Ji-Soo, Lee, Yejin, Shin, Teo Jeon, Hyun, Hong-Keun, Kim, Young-Jae, Kim, Jung-Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947619/
https://www.ncbi.nlm.nih.gov/pubmed/35327801
http://dx.doi.org/10.3390/children9030429

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947619/
https://www.ncbi.nlm.nih.gov/pubmed/35327801
http://dx.doi.org/10.3390/children9030429

Ejemplares similares