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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Kamamoto, Munefumi, Machida, Junichiro, Yamaguchi, Seishi, Kimura, Masashi, Ono, Takao, Jezewski, Peter A, Higashi, Yujiro, Nakayama, Atsuo, Shimozato, Kazuo, Tokita, Yoshihito
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group 2011
Pynciau:
Article
Mynediad Ar-lein: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
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg