FAM83H Mutations in Families with Autosomal-Dominant Hypocalcified Amelogenesis Imperfecta

Amelogenesis imperfecta (AI) is a collection of diverse inherited disorders featuring dental-enamel defects in the absence of significant nondental symptoms. AI phenotypes vary and are categorized as hypoplastic, hypocalcified, and hypomaturation types. Phenotypic specificity to enamel has focused r...

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Detalhes bibliográficos
Main Authors: Kim, Jung-Wook, Lee, Sook-Kyung, Lee, Zang Hee, Park, Joo-Cheol, Lee, Kyung-Eun, Lee, Myoung-Hwa, Park, Jong-Tae, Seo, Byoung-Moo, Hu, Jan C.-C., Simmer, James P.
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2008
Assuntos:
Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2427219/
https://ncbi.nlm.nih.gov/pubmed/18252228
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2007.09.020
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