Pages that link to "ROMK"
← ROMK
Showing 50 items.
- Shaker (gene) (links | edit)
- Liddle's syndrome (links | edit)
- Bartter syndrome (links | edit)
- Ion transporter (links | edit)
- TRPV6 (links | edit)
- Vitelliform macular dystrophy (links | edit)
- Congenital absence of the vas deferens (links | edit)
- Aquaporin-4 (links | edit)
- Aquaporin-2 (links | edit)
- Pseudohypoaldosteronism (links | edit)
- Epithelial sodium channel (links | edit)
- Mucolipidosis type IV (links | edit)
- Aquaporin-3 (links | edit)
- Aquaporin-1 (links | edit)
- Kv1.1 (links | edit)
- Calcium-activated potassium channel (links | edit)
- Voltage-gated potassium channel (links | edit)
- Two-pore-domain potassium channel (links | edit)
- Cation channels of sperm (links | edit)
- Two-pore channel (links | edit)
- Generalized epilepsy with febrile seizures plus (links | edit)
- Nav1.4 (links | edit)
- SCN5A (links | edit)
- Cav1.2 (links | edit)
- Kir2.1 (links | edit)
- KCNE1 (links | edit)
- Benign familial neonatal seizures (links | edit)
- Pacemaker current (links | edit)
- ATP-sensitive potassium channel (links | edit)
- Innexin (links | edit)
- Catecholaminergic polymorphic ventricular tachycardia (links | edit)
- SK channel (links | edit)
- Spinocerebellar ataxia type 6 (links | edit)
- Episodic ataxia (links | edit)
- Spinocerebellar ataxia type-13 (links | edit)
- Congenital stationary night blindness (links | edit)
- Sodium voltage-gated channel alpha subunit 9 (links | edit)
- Familial atrial fibrillation (links | edit)
- Dent's disease (links | edit)
- TRPV1 (links | edit)
- TRPC (links | edit)
- TRPV (links | edit)
- TRPM (links | edit)
- R-type calcium channel (links | edit)
- Q-type calcium channel (links | edit)
- P-type calcium channel (links | edit)
- N-type calcium channel (links | edit)
- L-type calcium channel (links | edit)
- Kir6.2 (links | edit)
- Membrane channel (links | edit)