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Innovative Therapeutic Approaches for the Treatment of the Ocular Morbidities in Patients with EEC Syndrome

Ectrodactyly-Ectodermal dysplasia-Clefting (EEC) syndrome is caused by heterozygous missense point mutations in the p63 gene, an important transcription factor during embryogenesis and for stem cell differentiation in stratified epithelia. Most of the cases are sporadic, related to de novo mutations...

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Detalles Bibliográficos
Autores principales: Barbaro, Vanessa, Bonelli, Filippo, Ferrari, Stefano, La Vella, Giulia, Di Iorio, Enzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9914602/
https://www.ncbi.nlm.nih.gov/pubmed/36766837
http://dx.doi.org/10.3390/cells12030495

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