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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Sci Rep
Prif Awduron: Ohyama, Yoshio, Lin, Ju-Hsien, Govitvattana, Nattanan, Lin, I-Ping, Venkitapathi, Sundharamani, Alamoudi, Ahmed, Husein, Dina, An, Chunying, Hotta, Hak, Kaku, Masaru, Mochida, Yoshiyuki
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group 2016
Pynciau:
Article
Mynediad Ar-lein: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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