A novel MSX1 mutation in hypodontia
Copyright policy )A novel MSX1 mutation in hypodontia
AbstractMSX1 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 Gln187Stop) in three individuals of one family. © 2004 Wiley‐Liss, Inc.
- Catholic University of America United States
- KU Leuven Belgium
Homeodomain Proteins, MSX1 Transcription Factor, Male, Base Sequence, Genetic Linkage, Cleft Lip, DNA Mutational Analysis, Cleft Palate, Radiography, Mutation, Humans, Female, Sequence Analysis, Anodontia, Genes, Dominant
Homeodomain Proteins, MSX1 Transcription Factor, Male, Base Sequence, Genetic Linkage, Cleft Lip, DNA Mutational Analysis, Cleft Palate, Radiography, Mutation, Humans, Female, Sequence Analysis, Anodontia, Genes, Dominant
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