Código QR

Identification of a Novel <i>FAM83H</i> 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...

Descrición completa

Gardado en:
Principais autores: Ji-Soo Song, Yejin Lee, Teo Jeon Shin, Hong-Keun Hyun, Young-Jae Kim, Jung-Wook Kim
Formato: Artigo
Idioma:Inglês
Publicado: MDPI AG 2022-03-01
Series:Children
Assuntos:
amelogenesis imperfecta
hypocalcified
general anesthesia
stainless steel crown
zirconia crown
<i>FAM83H</i>
Acceso en liña:https://www.mdpi.com/2227-9067/9/3/429
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares