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Novel FAM83H mutations in patients with amelogenesis imperfecta

Amelogenesis imperfecta (AI), characterized by a deficiency in the quantity and/or quality of dental enamel, is genetically heterogeneous and phenotypically variable. The most severe type, hypocalcified AI, is mostly caused by truncating mutations in the FAM83H gene. This study aimed to identify gen...

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Detaylı Bibliyografya
Yayımlandı:Sci Rep
Asıl Yazarlar: Xin, Wang, Wenjun, Wang, Man, Qin, Yuming, Zhao
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group UK 2017
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5519741/
https://ncbi.nlm.nih.gov/pubmed/28729668
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-05208-0
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