(Q28219109)
Statements
A naturally occurring mutation in the SLC21A6 gene causing impaired membrane localization of the hepatocyte uptake transporter (English)
Ulrich M Zanger
Christoph Michalski
Andreas K Nuessler
Kathrin Klein
Michel Eichelbaum
Dietrich Keppler
Jorg Konig
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Identifiers
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2 references