The Usher syndrome 1C protein harmonin regulates canonical Wnt signaling

Human Usher syndrome (USH) is the most common form of hereditary combined deaf-blindness. USH is a complex genetic disorder, and the pathomechanisms underlying the disease are far from being understood, especially in the eye and retina. The USH1C gene encodes the scaffold protein harmonin which orga...

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Detalles Bibliográficos
Autores principales: Schäfer, Jessica, Wenck, Nicole, Janik, Katharina, Linnert, Joshua, Stingl, Katarina, Kohl, Susanne, Nagel-Wolfrum, Kerstin, Wolfrum, Uwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944737/
https://www.ncbi.nlm.nih.gov/pubmed/36846582
http://dx.doi.org/10.3389/fcell.2023.1130058

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944737/
https://www.ncbi.nlm.nih.gov/pubmed/36846582
http://dx.doi.org/10.3389/fcell.2023.1130058

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