Misplaced Pages

The following pages link to Solute carrier family

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Showing 50 items.

• Biological membrane (links | edit)
• Endocytosis (links | edit)
• Facilitated diffusion (links | edit)
• Genetic disorder (links | edit)
• Phenylketonuria (links | edit)
• Zinc (links | edit)
• Dopamine (links | edit)
• Crohn's disease (links | edit)
• Exocytosis (links | edit)
• Active transport (links | edit)
• Alkaptonuria (links | edit)
• Glycoprotein (links | edit)
• Congenital disorder of glycosylation (links | edit)
• Phagocytosis (links | edit)
• Butyric acid (links | edit)
• SLC (links | edit)
• List of gene families (links | edit)
• Passive transport (links | edit)
• Serotonin transporter (links | edit)
• Thermogenin (links | edit)
• Membrane transport protein (links | edit)
• Methylmalonic acidemias (links | edit)
• Propionic acidemia (links | edit)
• Hyperammonemia (links | edit)
• Lysosomal storage disease (links | edit)
• Waardenburg syndrome (links | edit)
• Membrane transport (links | edit)
• Homocystinuria (links | edit)
• Fructose malabsorption (links | edit)
• Hyperinsulinemic hypoglycemia (links | edit)
• Alpha-mannosidosis (links | edit)
• Pharmacogenomics (links | edit)
• Uniporter (links | edit)
• Antiporter (links | edit)
• Cystinuria (links | edit)
• Pinocytosis (links | edit)
• Ornithine transcarbamylase deficiency (links | edit)
• Inborn errors of metabolism (links | edit)
• Champagne gene (links | edit)
• Pendred syndrome (links | edit)
• Fatty acid metabolism (links | edit)
• Diastrophic dysplasia (links | edit)
• Atelosteogenesis, type II (links | edit)
• Receptor-mediated endocytosis (links | edit)
• Trimethylaminuria (links | edit)
• Fuchs' dystrophy (links | edit)
• Isovaleric acidemia (links | edit)
• Maple syrup urine disease (links | edit)
• Dopamine transporter (links | edit)
• Cystinosis (links | edit)