Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders

Tooth development is a complex process that involves precise and time-dependent orchestration of multiple genetic, molecular, and cellular interactions. Ameloblastin (AMBN, also named “amelin” or “sheathlin”) is the second most abundant enamel matrix protein known to have a key role in amelogenesis....

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Detalhes bibliográficos
Publicado no:Int J Oral Sci
Main Authors: Lu, Ting, Li, Meiyi, Xu, Xiangmin, Xiong, Jun, Huang, Cheng, Zhang, Xuelian, Hu, Aiqin, Peng, Ling, Cai, Decheng, Zhang, Leitao, Wu, Buling, Xiong, Fu
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2018
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6119682/
https://ncbi.nlm.nih.gov/pubmed/30174330
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41368-018-0027-9
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