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Mutations in ATP6AP2 cause autophagic liver disease in humans
The biogenesis of the proton pump V-ATPase commences with the assembly of the proton pore sector V(0) in the endoplasmic reticulum (ER). This process occurs under the control of a group of assembly factors whose mutations have recently been shown to cause glycosylation disorders with overlapping phe...
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| Veröffentlicht in: | Autophagy |
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| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Taylor & Francis
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6103403/ https://ncbi.nlm.nih.gov/pubmed/29388887 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15548627.2018.1434370 |
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