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Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2).
van den Heuvel LP, Assink K, Willemsen M, Monnens L. van den Heuvel LP, et al. Among authors: assink k. Hum Genet. 2002 Dec;111(6):544-7. doi: 10.1007/s00439-002-0820-5. Epub 2002 Sep 27. Hum Genet. 2002. PMID: 12436245
Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiency.
Assink K, Schiphorst R, Allford S, Karpman D, Etzioni A, Brichard B, van de Kar N, Monnens L, van den Heuvel L. Assink K, et al. Kidney Int. 2003 Jun;63(6):1995-9. doi: 10.1046/j.1523-1755.63.6s.1.x. Kidney Int. 2003. PMID: 12753286 Free article.
Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunit.
Meij IC, Koenderink JB, van Bokhoven H, Assink KF, Groenestege WT, de Pont JJ, Bindels RJ, Monnens LA, van den Heuvel LP, Knoers NV. Meij IC, et al. Among authors: assink kf. Nat Genet. 2000 Nov;26(3):265-6. doi: 10.1038/81543. Nat Genet. 2000. PMID: 11062458
T-cell responses to neurofilament light protein are part of the normal immune repertoire.
Huizinga R, Hintzen RQ, Assink K, van Meurs M, Amor S. Huizinga R, et al. Among authors: assink k. Int Immunol. 2009 Apr;21(4):433-41. doi: 10.1093/intimm/dxp011. Epub 2009 Feb 24. Int Immunol. 2009. PMID: 19240089