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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...
שמור ב:
| הוצא לאור ב: | J Proteome Res |
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| Main Authors: | , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Chemical
Society
2021
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| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8280732/ https://ncbi.nlm.nih.gov/pubmed/34027671 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.jproteome.1c00126 |
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