Pages that link to "SCNN1G"
← SCNN1G
Showing 50 items.
- Genetic disorder (links | edit)
- Ion channel (links | edit)
- Neuromyotonia (links | edit)
- Cystic fibrosis (links | edit)
- Febrile seizure (links | edit)
- Brugada syndrome (links | edit)
- Gap junction (links | edit)
- Aquaporin (links | edit)
- Long QT syndrome (links | edit)
- BK channel (links | edit)
- Osteopetrosis (links | edit)
- Membrane transport protein (links | edit)
- Arrhythmogenic cardiomyopathy (links | edit)
- Congenital insensitivity to pain (links | edit)
- Malignant hyperthermia (links | edit)
- Erythromelalgia (links | edit)
- Hallermann–Streiff syndrome (links | edit)
- Potassium channel (links | edit)
- Hyperkalemic periodic paralysis (links | edit)
- Transient receptor potential channel (links | edit)
- Porin (protein) (links | edit)
- Timothy syndrome (links | edit)
- Connexin (links | edit)
- Inositol trisphosphate receptor (links | edit)
- Cystic fibrosis transmembrane conductance regulator (links | edit)
- Voltage-gated ion channel (links | edit)
- Ligand-gated ion channel (links | edit)
- Calcium channel (links | edit)
- Chloride channel (links | edit)
- Jervell and Lange-Nielsen syndrome (links | edit)
- Romano–Ward syndrome (links | edit)
- Andersen–Tawil syndrome (links | edit)
- KvLQT1 (links | edit)
- Voltage-gated calcium channel (links | edit)
- Hypoplastic left heart syndrome (links | edit)
- Ryanodine receptor (links | edit)
- HERG (links | edit)
- Channelopathy (links | edit)
- ROMK (links | edit)
- Myotonia congenita (links | edit)
- Inward-rectifier potassium channel (links | edit)
- Sodium channel (links | edit)
- Transporter Classification Database (links | edit)
- Hypokalemic periodic paralysis (links | edit)
- Paramyotonia congenita (links | edit)
- Nephrogenic diabetes insipidus (links | edit)
- Magnesium transporter (links | edit)
- Shaker (gene) (links | edit)
- Liddle's syndrome (links | edit)
- Bartter syndrome (links | edit)