FAM20A binds to and regulates FAM20C localization

Mutations in the Family with sequence similarity (FAM) 20 gene family are associated with mineralized tissue phenotypes in humans. Among these genes, FAM20A mutations are associated with Amelogenesis Imperfecta (AI) with gingival hyperplasia and nephrocalcinosis, while FAM20C mutations cause Raine s...

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Detalles Bibliográficos
Autores principales: Ohyama, Yoshio, Lin, Ju-Hsien, Govitvattana, Nattanan, Lin, I-Ping, Venkitapathi, Sundharamani, Alamoudi, Ahmed, Husein, Dina, An, Chunying, Hotta, Hak, Kaku, Masaru, Mochida, Yoshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4904241/
https://www.ncbi.nlm.nih.gov/pubmed/27292199
http://dx.doi.org/10.1038/srep27784

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4904241/
https://www.ncbi.nlm.nih.gov/pubmed/27292199
http://dx.doi.org/10.1038/srep27784

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