An Aberrant Splice Acceptor Site Due to a Novel Intronic Nucleotide Substitution in MSX1 Gene Is the Cause of Congenital Tooth Agenesis in a Japanese Family-Reference-Cited by-同舟云学术

An Aberrant Splice Acceptor Site Due to a Novel Intronic Nucleotide Substitution in MSX1 Gene Is the Cause of Congenital Tooth Agenesis in a Japanese Family

Published:2015-06-01 Issue:6 Volume:10 Page:e0128227
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Tatematsu Tadashi,Kimura Masashi,Nakashima Mitsuko,Machida Junichiro,Yamaguchi Seishi,Shibata Akio,Goto Hiroki,Nakayama Atsuo,Higashi Yujiro,Miyachi Hitoshi,Shimozato Kazuo,Matsumoto Naomichi,Tokita Yoshihito

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference30 articles.

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5. A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia?;A Mostowska;J Appl Genet,2006

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4. Characterization of novel MSX1 variants causally associated with non‐syndromic oligodontia in Chinese families;Molecular Genetics & Genomic Medicine;2023-12-08

5. Novel WNT10A variant in a Japanese case of nonsyndromic oligodontia;Human Genome Variation;2023-01-26