TY - JOUR AU - Yahyaoui, Raquel AU - Pérez-Frías, Javier PY - 2019 DO - 10.3390/ijms21010119 UR - http://hdl.handle.net/10668/3627 T2 - International Journal of Molecular Sciences AB - Amino acid transporters play very important roles in nutrient uptake, neurotransmitter recycling, protein synthesis, gene expression, cell redox balance, cell signaling, and regulation of cell volume. With regard to transporters that are closely... LA - en PB - MDPI KW - SLC KW - Solute carriers KW - Membrane transport KW - Inborn errors of metabolism KW - Amino acid transporter KW - Symporter KW - Inherited metabolic disorders KW - Proteínas transportadoras de solutos KW - Errores innatos del metabolismo KW - Sistemas de transporte de aminoácidos KW - Simportadores KW - Encefalopatías metabólicas innatas KW - Medical Subject Headings::Phenomena and Processes::Metabolic Phenomena::Metabolism::Biological Transport::Biological Transport, Active KW - Medical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans KW - Medical Subject Headings::Phenomena and Processes::Cell Physiological Phenomena::Cell Physiological Processes::Signal Transduction KW - Medical Subject Headings::Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Carrier Proteins::Membrane Transport Proteins::Amino Acid Transport Systems KW - Medical Subject Headings::Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Amino Acids KW - Medical Subject Headings::Diseases::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Metabolism, Inborn Errors KW - Medical Subject Headings::Diseases::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Metabolism, Inborn Errors::Brain Diseases, Metabolic, Inborn KW - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes KW - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Phenotype TI - Amino Acid Transport Defects in Human Inherited Metabolic Disorders TY - review article ER -