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Mutant MESD links cellular stress to type I collagen aggregation in osteogenesis imperfecta type XX
Aberrant forms of endoplasmic reticulum (ER)-resident chaperones are implicated in loss of protein quality control in rare diseases. Here we report a novel mutation (p.Asp233Asn) in the ER retention signal of MESD by whole exome sequencing of an individual diagnosed with osteogenesis imperfecta (OI)...
Tallennettuna:
| Julkaisussa: | Matrix Biol |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2023
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7615836/ https://ncbi.nlm.nih.gov/pubmed/36526215 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.matbio.2022.12.001 |
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