Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia

Multiple previous reports confirm that several missense alleles of MSX1 exhibit Mendelian inheritance of an oligodontia phenotype (agenesis of more than six secondary teeth besides third molars). However, the extent to which missense MSX1 alleles contribute to common, multifactorial disorders is les...

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Detalhes bibliográficos
Main Authors: Kamamoto, Munefumi, Machida, Junichiro, Yamaguchi, Seishi, Kimura, Masashi, Ono, Takao, Jezewski, Peter A, Higashi, Yujiro, Nakayama, Atsuo, Shimozato, Kazuo, Tokita, Yoshihito
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2011
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3172929/
https://ncbi.nlm.nih.gov/pubmed/21448236
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2011.47
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