An allelic series ofTrp63mutations defines TAp63 as a modifier of EEC syndrome
Author:
Affiliation:
1. Cold Spring Harbor Laboratory; Cold Spring Harbor; New York
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36074/fullpdf
Reference25 articles.
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2. Differential altered stability and transcriptional activity of DeltaNp63 mutants in distinct ectodermal dysplasias;Browne;J Cell Sci,2011
3. Palatogenesis: Morphogenetic and molecular mechanisms of secondary palate development;Bush;Development,2012
4. Twenty-four cases of the EEC syndrome: Clinical presentation and management;Buss;J Med Genet,1995
5. Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome;Celli;Cell,1999
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