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Exclusion of mutations in FXYD2, CLDN16 and SLC12A3 in two families with primary renal Mg2+ loss.
Meij, Iwan C; van den Heuvel, Lambert P W J; Hemmes, Sies; van der Vliet, Walter A; Willems, Johannes L; Monnens, Leo A H; Knoers, Nine V A M.
Affiliation
  • Meij IC; Department of Pediatrics, University Hospital Nijmegen, Nijmegen, The Netherlands.
Nephrol Dial Transplant ; 18(3): 512-6, 2003 Mar.
Article in En | MEDLINE | ID: mdl-12584272
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Database: MEDLINE Main subject: Receptors, Drug / Carrier Proteins / Sodium-Potassium-Exchanging ATPase / Symporters / Kidney Diseases / Magnesium / Membrane Proteins / Mutation Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Nephrol Dial Transplant Journal subject: NEFROLOGIA / TRANSPLANTE Year: 2003 Type: Article Affiliation country: Netherlands
Search on Google
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PubMed Links

Database: MEDLINE Main subject: Receptors, Drug / Carrier Proteins / Sodium-Potassium-Exchanging ATPase / Symporters / Kidney Diseases / Magnesium / Membrane Proteins / Mutation Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Nephrol Dial Transplant Journal subject: NEFROLOGIA / TRANSPLANTE Year: 2003 Type: Article Affiliation country: Netherlands