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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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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Xin, Wang, Wenjun, Wang, Man, Qin, Yuming, Zhao
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2017
Assuntos:
Acesso em linha: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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