Cystinuria-specific rBAT(R365W) mutation reveals two translocation pathways in the amino acid transporter rBAT-b 0,+ AT
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Authors
Pineda, Marta
Wagner, Carsten
Broer, Angelika
Stehberger, Paul
Kaltenbach, Simone
Gaskett, Chris
Martin del Rio, Rafael
Zorzano, Antonio
Palacin, Manuel
Lang, Florian
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Portland Press
Abstract
Apical reabsorption of dibasic amino acids and cystine in kidney is mediated by the heteromeric amino acid antiporter rBAT/b0,+AT (system b0,+). Mutations in rBAT cause cystinuria type A, whereas mutations in b0,+AT cause cystinuria type B. b0,+AT is the
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Biochemical Journal