Pages that link to "VPS13B"
← VPS13B
Showing 50 items.
- Charcot–Marie–Tooth disease (links | edit)
- Congenital disorder of glycosylation (links | edit)
- Caveolae (links | edit)
- Hereditary spastic paraplegia (links | edit)
- Long QT syndrome (links | edit)
- Small GTPase (links | edit)
- Limb–girdle muscular dystrophy (links | edit)
- Clathrin (links | edit)
- COPII (links | edit)
- COPI (links | edit)
- Synaptic vesicle (links | edit)
- Rab (G-protein) (links | edit)
- Receptor-mediated endocytosis (links | edit)
- Caveolin (links | edit)
- Spinocerebellar ataxia (links | edit)
- SNARE protein (links | edit)
- Vesicle-associated membrane protein (links | edit)
- Synaptobrevin (links | edit)
- Chédiak–Higashi syndrome (links | edit)
- Retromer (links | edit)
- Transporter Classification Database (links | edit)
- Chromosome 8 (links | edit)
- Hermansky–Pudlak syndrome (links | edit)
- Choroideremia (links | edit)
- Cohen syndrome (links | edit)
- Dynamin (links | edit)
- Griscelli syndrome (links | edit)
- ADP ribosylation factor (links | edit)
- SNAP25 (links | edit)
- Synaptotagmin (links | edit)
- Caveolin 3 (links | edit)
- Archain (links | edit)
- Coatomer (links | edit)
- Hemophagocytic lymphohistiocytosis (links | edit)
- Vesicular transport protein (links | edit)
- Lysosomal trafficking regulator (links | edit)
- STX11 (links | edit)
- COH1 (redirect page) (links | edit)
- Caveolin 1 (links | edit)
- STX1A (links | edit)
- COPB1 (links | edit)
- DNM2 (links | edit)
- RAB3A (links | edit)
- STX4 (links | edit)
- SYT1 (links | edit)
- Biogenesis of lysosome-related organelles complex 1 (links | edit)
- CLTC (links | edit)
- DNM1 (links | edit)
- VAMP2 (links | edit)
- LMAN1 (links | edit)