Characterization of Novel MSX1 Mutations Identified in Japanese Patients with Nonsyndromic Tooth Agenesis-Reference-Cited by-同舟云学术

Characterization of Novel MSX1 Mutations Identified in Japanese Patients with Nonsyndromic Tooth Agenesis

Published:2014-08-07 Issue:8 Volume:9 Page:e102944
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Yamaguchi Seishi,Machida Junichiro,Kamamoto Munefumi,Kimura Masashi,Shibata Akio,Tatematsu Tadashi,Miyachi Hitoshi,Higashi Yujiro,Jezewski Peter,Nakayama Atsuo,Shimozato Kazuo,Tokita Yoshihito

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference43 articles.

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2. Mutation of PAX9 is associated with oligodontia;DW Stockton;Nat Genet,2000

3. MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans;MJ van den Boogaard;Nat Genet,2000

4. A nonsense mutation in MSX1 causes Witkop syndrome;D Jumlongras;Am J Hum Genet,2001

5. Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia;P Das;Hum Genet,2002

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