Pages that link to "SLC2A10"

Showing 50 items.

• Genetic disorder (links | edit)
• Crohn's disease (links | edit)
• Congenital disorder of glycosylation (links | edit)
• Serotonin transporter (links | edit)
• Thermogenin (links | edit)
• Membrane transport protein (links | edit)
• Fructose malabsorption (links | edit)
• Hyperinsulinemic hypoglycemia (links | edit)
• Uniporter (links | edit)
• Cystinuria (links | edit)
• Pendred syndrome (links | edit)
• Diastrophic dysplasia (links | edit)
• Atelosteogenesis, type II (links | edit)
• Fuchs' dystrophy (links | edit)
• Dopamine transporter (links | edit)
• Gitelman syndrome (links | edit)
• Norepinephrine transporter (links | edit)
• Hartnup disease (links | edit)
• Salla disease (links | edit)
• Lysinuric protein intolerance (links | edit)
• GLUT2 (links | edit)
• Glucose transporter (links | edit)
• Prestin (links | edit)
• Hereditary elliptocytosis (links | edit)
• Achondrogenesis type 1B (links | edit)
• Band 3 anion transport protein (links | edit)
• Transporter Classification Database (links | edit)
• Ferroportin (links | edit)
• African iron overload (links | edit)
• Nonsyndromic deafness (links | edit)
• Sodium/potassium/calcium exchanger 5 (links | edit)
• GLUT4 (links | edit)
• Glutamate transporter (links | edit)
• Autosomal recessive multiple epiphyseal dysplasia (links | edit)
• Acrodermatitis enteropathica (links | edit)
• Ion transporter (links | edit)
• Testicular microlithiasis (links | edit)
• Vesicular monoamine transporter 2 (links | edit)
• Vesicular monoamine transporter 1 (links | edit)
• Karyopherin (links | edit)
• Importin (links | edit)
• GLUT1 (links | edit)
• Solute carrier family (links | edit)
• CD98 (links | edit)
• Excitatory amino acid transporter 5 (links | edit)
• Excitatory amino acid transporter 4 (links | edit)
• Sodium-glucose transport proteins (links | edit)
• Na–K–Cl cotransporter (links | edit)
• Sodium-chloride symporter (links | edit)
• Multiple epiphyseal dysplasia (links | edit)