Cargando…
Amnionless-mediated glycosylation is crucial for cell surface targeting of cubilin in renal and intestinal cells
Mutations in either cubilin (CUBN) or amnionless (AMN) genes cause Imerslund–Gräsbeck syndrome (IGS), a hereditary disease characterised by anaemia attributed to selective intestinal malabsorption of cobalamin and low-molecular weight proteinuria. Although cubilin protein does not have a transmembra...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799345/ https://www.ncbi.nlm.nih.gov/pubmed/29402915 http://dx.doi.org/10.1038/s41598-018-20731-4 |