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• W2011269462 abstract "In the late 1990s, the identification of transporters and transporter-associated genes progressed substantially due to the development of new cloning approaches such as expression cloning and, subsequently, to the implementation of the human genome project. Since then, the role of many transporter genes in human diseases has been elucidated. In this overview, we focus on inherited disorders of epithelial transporters. In particular, we review genetic defects of the genes encoding glucose transporters (SLC2 and SLC5 families) and amino acid transporters (SLC1, SLC3, SLC6 and SLC7 families)." @default.
• W2011269462 created "2016-06-24" @default.
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• W2011269462 date "2008-04-01" @default.
• W2011269462 modified "2023-10-05" @default.
• W2011269462 title "Inherited epithelial transporter disorders—an overview" @default.
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• W2011269462 doi "https://doi.org/10.1007/s10545-008-0861-6" @default.
• W2011269462 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18415698" @default.
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