WNT10Amutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations
Author:
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; Jönköping Sweden
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36243/fullpdf
Reference29 articles.
1. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia;Adaimy;Am J Hum Genet,2007
2. Signs and symptoms from ectodermal organs in young Swedish individuals with oligodontia;Bergendal;Int J Paediatr Dent,2006
3. Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes;Bergendal;Am J Med Genet Part A,2011
4. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes;Bohring;Am J Hum Genet,2009
5. Multiple sequence alignment with the Clustal series of programs;Chenna;Nucleic Acids Res,2003
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