ID Database Citation
9783642403361 ISBN "Physician’s Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases [Internet]. Blau N, Duran M, Gibson KM, Dionisi-Vici C. Springer; 2014. 0 p. Available from: https://books.google.com/books/about/Physician_s_Guide_to_the_Diagnosis_Treat.html?hl=&id=wJRBnwEACAAJ OpenLibrary Worldcat"
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19185582 Pubmed "Tissue-specific amino acid transporter partners ACE2 and collectrin differentially interact with hartnup mutations. Camargo SMR, Singer D, Makrides V, Huggel K, Pos KM, Wagner CA, et al. Gastroenterology. 2009 Mar;136(3):872–82. PubMed Europe PMC Scholia"
21123949 Pubmed "Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria. Bailey CG, Ryan RM, Thoeng AD, Ng C, King K, Vanslambrouck JM, et al. J Clin Invest. 2011 Jan;121(1):446–53. PubMed Europe PMC Scholia"
26690923 Pubmed "Caveolin-1 Sensitivity of Excitatory Amino Acid Transporters EAAT1, EAAT2, EAAT3, and EAAT4. Abousaab A, Warsi J, Elvira B, Lang F. J Membr Biol. 2016 Jun;249(3):239–49. PubMed Europe PMC Scholia"