Prevalence of WNT10A gene mutations in non-syndromic oligodontia
Author:
Funder
Deutsche Gesellschaft für Kieferorthopädie
Publisher
Springer Science and Business Media LLC
Subject
General Dentistry
Link
http://link.springer.com/article/10.1007/s00784-018-2731-4/fulltext.html
Reference48 articles.
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3. Visinoni AF, de Souza RL, Freire-Maia N, Gollop TR, Chautard-Freire-Maia EA (2003) X-linked hypohidrotic ectodermal dysplasia mutations in Brazilian families. Am J Med Genet A 122A:51–55. https://doi.org/10.1002/ajmg.a.20276
4. Clauss F, Maniere MC, Obry F, Waltmann E, Hadj-Rabia S, Bodemer C, Alembik Y, Lesot H, Schmittbuhl M (2008) Dento-craniofacial phenotypes and underlying molecular mechanisms in hypohidrotic ectodermal dysplasia (HED): a review. J Dent Res 87:1089–1099
5. Kratochwil K, Galceran J, Tontsch S, Roth W, Grosschedl R (2002) FGF4, a direct target of LEF1 and Wnt signaling, can rescue the arrest of tooth organogenesis in Lef1(-/-) mice. Genes Dev 16:3173–3185. https://doi.org/10.1101/gad.1035602.
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