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Disordered FGF23 and mineral metabolism in children with CKD.
Portale AA, Wolf M, Jüppner H, Messinger S, Kumar J, Wesseling-Perry K, Schwartz GJ, Furth SL, Warady BA, Salusky IB. Portale AA, et al. Clin J Am Soc Nephrol. 2014 Feb;9(2):344-53. doi: 10.2215/CJN.05840513. Epub 2013 Dec 5. Clin J Am Soc Nephrol. 2014. PMID: 24311704 Free PMC article.
A novel missense mutation in SLC34A3 that causes hereditary hypophosphatemic rickets with hypercalciuria in humans identifies threonine 137 as an important determinant of sodium-phosphate cotransport in NaPi-IIc.
Jaureguiberry G, Carpenter TO, Forman S, Jüppner H, Bergwitz C. Jaureguiberry G, et al. Am J Physiol Renal Physiol. 2008 Aug;295(2):F371-9. doi: 10.1152/ajprenal.00090.2008. Epub 2008 May 14. Am J Physiol Renal Physiol. 2008. PMID: 18480181 Free PMC article.