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Allele-specific silencing of EEC p63 mutant R304W restores p63 transcriptional activity
EEC (ectrodactily-ectodermal dysplasia and cleft lip/palate) syndrome is a rare genetic disease, autosomal dominant inherited. It is part of the ectodermal dysplasia disorders caused by heterozygous mutations in TP63 gene. EEC patients present limb malformations, orofacial clefting, skin and skin...
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| Publicado no: | Cell Death Dis |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4917656/ https://ncbi.nlm.nih.gov/pubmed/27195674 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/cddis.2016.118 |
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