Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia-Reference-Cited by-同舟云学术

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

Published:2011-03-30 Issue:8 Volume:19 Page:844-850
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Kamamoto Munefumi,Machida Junichiro,Yamaguchi Seishi,Kimura Masashi,Ono Takao,Jezewski Peter A,Higashi Yujiro,Nakayama Atsuo,Shimozato Kazuo,Tokita Yoshihito

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg201147.pdf

Reference62 articles.

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3. Jumlongras D, Bei M, Stimson JM et al: A nonsense mutation in MSX1 causes Witkop syndrome. Am J Hum Genet 2001; 69: 67–74.

4. Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE : A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nat Genet 1996; 13: 417–421.

5. van den Boogaard MJ, Dorland M, Beemer FA, van Amstel HK : MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nat Genet 2000; 24: 342–343.

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