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Singer D, Camargo SM, Huggel K, Romeo E, Danilczyk U, Kuba K, Chesnov S, Caron MG, Penninger JM, Verrey F.SourceInstitute of Physiology and Center for Integrative Human Physiology, University of Zurich, 8057 Zurich, Switzerland.
The Journal of biological chemistry.J Biol Chem.2009 Jul 24;284(30):19953-60. Epub 2009 May 28.
The orphan transporter Slc6a18 (XT2) is highly expressed at the luminal membrane of kidney proximal tubules and displays approximately 50% identity with Slc6a19 (B(0)AT1), which is the main neutral amino acid transporter in both kidney and small intestine. As yet, the amino acid transport function o
PMID 19478081

Hypophosphataemic osteomalacia due to de Toni-Debre-Fanconi syndrome in a 19-year old girl.

Tsilchorozidou T, Yovos JG.SourceDivision of Endocrinology, Diabetes and Metabolism, AHEPA University Hospital, Thessaloniki, Greece. tasoula@med.auth.gr
Hormones (Athens, Greece).Hormones (Athens).2005 Jul-Sep;4(3):171-6.
Osteomalacia associated with adult onset Fanconi syndrome is thought to result from hypophosphataemia due to renal phosphate loss and relative 1,25-dihydroxyvitamin D3 deficiency. In this disorder, the impaired renal phosphate uptake occurs as part of a generalized tubular defect in association with
PMID 16613828