4.2 Article

A novel MSX1 mutation in hypodontia

Journal

AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 128A, Issue 4, Pages 401-403

Publisher

WILEY
DOI: 10.1002/ajmg.a.30181

Keywords

MSX1; PAX9; oligodontia; autosomal dominant

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MSX1 mutations have been reported in four unrelated families with autosomal dominant tooth agenesis. In one family, some individuals also had cleft lip and/or palate. We have identified a novel MSX1 mutation (559 C --> T, resulting in G1n187Stop) in three individuals of one family. (C) 2004 Wiley-Liss, Inc.

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