Identification of the C-terminal region in Amelogenesis Imperfecta causative protein WDR72 required for Golgi localization

Amelogenesis Imperfecta (AI) represents a group of hereditary conditions that manifest tooth enamel defects. Several causative mutations in the WDR72 gene have been identified and patients with WDR72 mutations have brown (or orange-brown) discolored enamel, rough enamel surface, early loss of enamel...

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Detalles Bibliográficos
Autores principales: Husein, Dina, Alamoudi, Ahmed, Ohyama, Yoshio, Mochida, Hanna, Ritter, Brigitte, Mochida, Yoshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930991/
https://www.ncbi.nlm.nih.gov/pubmed/35301423
http://dx.doi.org/10.1038/s41598-022-08719-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930991/
https://www.ncbi.nlm.nih.gov/pubmed/35301423
http://dx.doi.org/10.1038/s41598-022-08719-7

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