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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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4904241/
https://ncbi.nlm.nih.gov/pubmed/27292199
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep27784
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