Imbalance of plasma amino acids, metabolites and lipids in patients with lysinuric protein intolerance (LPI)

Author:

Kurko Johanna,Tringham Maaria,Tanner Laura,Näntö-Salonen KirstiORCID,Vähä-Mäkilä Mari,Nygren Heli,Pöhö Päivi,Lietzen Niina,Mattila Ismo,Olkku Anu,Hyötyläinen Tuulia,Orešič Matej,Simell Olli,Niinikoski Harri,Mykkänen Juha

Publisher

Elsevier BV

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference61 articles.

1. Transport defects of amino acids at the cell membrane: cystinuria, lysinuric protein intolerance and hartnup disorder;Näntö-Salonen,2012

2. Identification of SLC7A7, encoding y+LAT-1, as the lysinuric protein intolerance gene;Torrents;Nat Genet,1999

3. Function and structure of heterodimeric amino acid transporters;Wagner;Am J Physiol Cell Physiol,2001

4. Carnitine deficiency and l-carnitine supplementation in lysinuric protein intolerance;Tanner;Metabolism,2008

5. Familial protein intolerance with deficient transport of basic amino acids. Report on an adult patient with chronic hyperammonemia;Kekomäki;Acta Med Scand,1968

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