Lysinuric protein intolerance: one gene, many problems
Author:
Publisher
American Physiological Society
Subject
Cell Biology,Physiology
Link
https://www.physiology.org/doi/pdf/10.1152/ajpcell.00166.2007
Reference21 articles.
1. SLC7A7, encoding a putative permease-related protein, is mutated in patients with lysinuric protein intolerance
2. The heterodimeric amino acid transporter 4F2hc/y+LAT2 mediates arginine efflux in exchange with glutamine
3. Growth hormone deficiency in a patient with lysinuric protein intolerance
4. Plasma Growth Hormone Response to Intravenous Administration of Amino Acids
5. Disorders of Amino-Acid Transport
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4. Prioritization of SNPs in y+LAT‐1 culpable of Lysinuric protein intolerance and their mutational impacts using protein‐protein docking and molecular dynamics simulation studies;Journal of Cellular Biochemistry;2019-06-18
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