Retinal Proteomics of a Mouse Model of Dystroglycanopathies Reveals Molecular Alterations in Photoreceptors

[Image: see text] Mutations in the POMT1 gene, encoding a protein O-mannosyltransferase essential for α-dystroglycan (α-DG) glycosylation, are frequently observed in a group of rare congenital muscular dystrophies, collectively known as dystroglycanopathies. However, it is hitherto unclear whether t...

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Detalles Bibliográficos
Autores principales: Uribe, Mary Luz, Martín-Nieto, José, Quereda, Cristina, Rubio-Fernández, Marcos, Cruces, Jesús, Janssen, George M. C., de Ru, Arnoud H., van Veelen, Peter A., Hensbergen, Paul J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280732/
https://www.ncbi.nlm.nih.gov/pubmed/34027671
http://dx.doi.org/10.1021/acs.jproteome.1c00126

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280732/
https://www.ncbi.nlm.nih.gov/pubmed/34027671
http://dx.doi.org/10.1021/acs.jproteome.1c00126

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