Mutation of PAX9 is associated with oligodontia
Copyright policy ) D W, Stockton; P, Das; M, Goldenberg; R N, D'Souza; P I, Patel;
Mutation of PAX9 is associated with oligodontia
We identified a frameshift mutation in the paired domain of PAX9 following genome-wide analysis of a family segregating autosomal dominant oligodontia. Affected members have normal primary dentition but lacked most permanent molars.
- The University of Texas Health Science Center at Houston United States
- Baylor College of Medicine United States
Male, Base Sequence, DNA, Pedigree, DNA-Binding Proteins, Mutation, Humans, Female, Amino Acid Sequence, PAX9 Transcription Factor, Polymorphism, Single-Stranded Conformational, Anodontia, Transcription Factors
Male, Base Sequence, DNA, Pedigree, DNA-Binding Proteins, Mutation, Humans, Female, Amino Acid Sequence, PAX9 Transcription Factor, Polymorphism, Single-Stranded Conformational, Anodontia, Transcription Factors
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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