Citations for
1ED12, ED3, EDA, EDAR, EDARADD, HEDAD, OODD, WNT10A
Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.
Cluzeau C, Hadj-Rabia S, Jambou M, Mansour S, Guigue P, Masmoudi S, Bal E, Chassaing N, Vincent MC, Viot G, Clauss F, Manière MC, Toupenay S, Le Merrer M, Lyonnet S, Cormier-Daire V, Amiel J, Faivre L, de Prost Y, Munnich A, Bonnefont JP, Bodemer C, Smahi A.
Hum Mutat 32(1):70-2. 2011
2OODD, WNT10A
WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome.
Nawaz S, Klar J, Wajid M, Aslam M, Tariq M, Schuster J, Baig SM, Dahl N.
Eur J Hum Genet 17(12):1600-5. Epub 2009 May 27.PMID: 19471313 2009
3WNT10A, OODD
Mutation in WNT10A Is Associated with an Autosomal Recessive Ectodermal Dysplasia: The Odonto-onycho-dermal Dysplasia.
Adaimy L, Chouery E, Megarbane H, Mroueh S, Delague V, Nicolas E, Belguith H, de Mazancourt P, Megarbane A.
Am J Hum Genet 81(4):821-8. Epub 2007 Aug 9. 2007