A novel missense mutation in the geneFZD6underlies autosomal recessive nail dysplasia
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2012.11203.x/fullpdf
Reference15 articles.
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2. Role of homeobox genes in the patterning, specification, and differentiation of ectodermal appendages in mammals;Duverger;J Cell Physiol,2008
3. Genetic interaction between Wnt/beta-catenin and BMP receptor signaling during formation of the AER and the dorsal-ventral axis in the limb;Soshnikova;Genes Dev,2003
4. FZD6 encoding the Wnt receptor frizzled 6 is mutated in autosomal-recessive nail dysplasia;Naz;Br J Dermatol,2012
5. Wnt/beta-catenin signaling in development and disease;Clevers;Cell,2006
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1. A novel pathogenic variant in the FZD6 gene causes recessive nail dysplasia in a Moroccan family;Clinical and Experimental Dermatology;2023-07-04
2. A possible founder mutation in FZD6 gene in a Turkish family with autosomal recessive nail dysplasia;BMC Medical Genetics;2019-01-14
3. Association of sequence variants in frizzled-6 with autosomal recessive nail dysplasia (NDNC-10) in Pashtun families;Journal of the Pakistan Medical Association;2019
4. A novel pathogenic variant in the FZD6 gene causes recessive nail dysplasia in a large Iranian kindred;Journal of Dermatological Science;2017-10
5. Genetics of Isolated Hereditary Nail Disorder;eLS;2017-09-15
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