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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Detaylı Bibliyografya
Yayımlandı:Sci Rep
Asıl Yazarlar: Ohyama, Yoshio, Lin, Ju-Hsien, Govitvattana, Nattanan, Lin, I-Ping, Venkitapathi, Sundharamani, Alamoudi, Ahmed, Husein, Dina, An, Chunying, Hotta, Hak, Kaku, Masaru, Mochida, Yoshiyuki
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group 2016
Konular:
Article
Online Erişim: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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