Llwytho...
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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | J Proteome Res |
|---|---|
| Prif Awduron: | , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
American Chemical
Society
2021
|
| Mynediad Ar-lein: | 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 |
| Tagiau: |
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