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WNT10A mutations account for ¼ of population‐based isolated oligodontia and show phenotypic correlations
Authors:Pakeeza Shaiq Arzoo  Joakim Klar  Birgitta Bergendal  Johanna Norderyd  Niklas Dahl
Affiliation:1. Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden;2. National Oral Disability Centre, The Institute for Postgraduate Dental Education, J?nk?ping, Sweden;3. Correspondence to: Niklas Dahl, M.D., Ph.D., Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, BMC, Box 815, 751 08 Uppsala, Sweden.;4. E‐mail:
Abstract:
Keywords:isolated oligodontia  WNT10A  mutation  genotype–  phenotype correlation
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