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...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Sci Rep
Hlavní autoři: Ohyama, Yoshio, Lin, Ju-Hsien, Govitvattana, Nattanan, Lin, I-Ping, Venkitapathi, Sundharamani, Alamoudi, Ahmed, Husein, Dina, An, Chunying, Hotta, Hak, Kaku, Masaru, Mochida, Yoshiyuki
Médium: Artigo
Jazyk:Inglês
Vydáno: Nature Publishing Group 2016
Témata:
Article
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky