WNT10A mutations account for 1/4 of population-based isolated oligodontia and show phenotypic correlations

American Journal of Medical Genetics, Part A

Volumn 164, Issue 2, 2014, Pages 353-359

  Arzoo, Pakeeza Shaiq ^a   Klar, Joakim ^a   Bergendal, Birgitta ^b   Norderyd, Johanna ^b   Dahl, Niklas ^a  

^a UPPSALA UNIVERSITY   (Sweden)

^b INSTITUTE FOR POSTGRADUATE DENTAL EDUCATION   (Sweden)

Author keywords

Genotype phenotype correlation; Isolated oligodontia; Mutation; WNT10A

Indexed keywords

ECTODYSPLASIN A; EDAR ASSOCIATED DEATH DOMAIN PROTEIN; TRANSCRIPTION FACTOR MSX1; TRANSCRIPTION FACTOR PAX9; WNT10A PROTEIN;

ARTICLE; AXIN2 GENE; COHORT ANALYSIS; CONTROLLED STUDY; DISEASE ASSOCIATION; EDA GENE; EDAR GENE; EDARADD GENE; FEMALE; GENE; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC IDENTIFICATION; GENETIC SCREENING; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MAJOR CLINICAL STUDY; MALE; MSX1 GENE; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; OLIGODONTIA; PAX9 GENE; PREVALENCE; PRIORITY JOURNAL; WNT10A GENE;

GENOTYPE-PHENOTYPE CORRELATION; ISOLATED OLIGODONTIA; MUTATION; WNT10A;

ALLELES; ANODONTIA; FEMALE; GENETIC ASSOCIATION STUDIES; GENOTYPE; HUMANS; MALE; MUTATION; PHENOTYPE; POPULATION SURVEILLANCE; SWEDEN; WNT PROTEINS;

EID: 84892875876     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36243     Document Type: Article

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