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Functional defect caused by the 4544G>A SNP in ABCC2

DOI

36

Citations

21

References

2011

Year

Laure Elens, Donatienne Tyteca, Nadtha Panin, Pierre J. Courtoy, Dominique Lison, Jean‐Baptiste Demoulin, Vincent Haufroid
Pharmacogenetics and Genomics

Abstract

The C1515Y amino acid substitution caused by the 4544G>A SNP in ABCC2 impairs its ATPase activity and is associated with higher cellular accumulation of ABCC2 substrates.

References

YearCitations

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