Autosomal Dominant Polycystic Kidney Disease Induced by Ciliary Defects
Autosomal dominant polycystic kidney disease (ADPKD) is a common genetic renal disease, which is caused by pathogenic mutations of either PKD1 (85%) or PKD2 (15%) genes, encoding for polycystin-1 (PC1) or polycystin-2 (PC2), respectively. These two proteins hetero-dimerize in renal primary cilia to...
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| Format: | Online |
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| Sprache: | Englisch |
| Veröffentlicht: |
Exon Publications
2024
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| Schlagworte: | |
| Online-Zugang: | https://directory.doabooks.org/handle/20.500.12854/136661 |
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