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Role and mechanism of chaperones calreticulin and ERP57 in restoring trafficking to mutant HERG-A561V protein
Long QT syndrome type 2 is caused by a mutation in the human-ether-a-go-go-related gene (HERG) gene encoding the rapidly activating delayed rectifier K-current. HERG is a key cell membrane glycoprotein; however, whether the maturation process of HERG protein involves key molecules derived from the c...
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| Yayımlandı: | Int J Mol Med |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
D.A. Spandidos
2021
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8262656/ https://ncbi.nlm.nih.gov/pubmed/34212985 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ijmm.2021.4992 |
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