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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Hlavní autoři: Kamamoto, Munefumi, Machida, Junichiro, Yamaguchi, Seishi, Kimura, Masashi, Ono, Takao, Jezewski, Peter A, Higashi, Yujiro, Nakayama, Atsuo, Shimozato, Kazuo, Tokita, Yoshihito
Médium: Artigo
Jazyk:Inglês
Vydáno: Nature Publishing Group 2011
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On-line přístup: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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