A novel missense mutation in the ectodysplasin-A (EDA) gene underlies X-linked recessive nonsyndromic hypodontia
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-4632.2010.04596.x/fullpdf
Reference18 articles.
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2. Mutation of PAX9 is associated with oligodontia;Stockton;Nat Genet,2000
3. A human MSX1 homeodomain missense mutation causes selective tooth agenesis;Vastardis;Nat Genet,1996
4. Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis;Mostowska;J Hum Genet,2006
5. A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia;Tao;J Hum Genet,2006
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1. The EDA/EDAR/NF-κB pathway in non-syndromic tooth agenesis: A genetic perspective;Frontiers in Genetics;2023-04-03
2. The influence of the inheritance on the occurrence of hypodontia and hyperdontia in children in the Federation of Bosnia and Herzegovina;Acta stomatologica Naissi;2022
3. Missense mutations in EDA and EDAR genes cause dominant syndromic tooth agenesis;Molecular Genetics & Genomic Medicine;2020-11-18
4. Nonsyndromic oligodontia;Journal of Orofacial Orthopedics / Fortschritte der Kieferorthopädie;2017-02-15
5. Genetic Implications in Orthodontic Tooth Movement;Biology of Orthodontic Tooth Movement;2016
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