Renal, Ocular, and Neuromuscular Involvements in Patients with CLDN19 Mutations

BACKGROUND AND OBJECTIVES: The objective of this study was to describe the renal and extrarenal findings in patients with recessively inherited familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) associated with CLDN19 mutations. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS...

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Detalhes bibliográficos
Main Authors: Faguer, Stanislas, Chauveau, Dominique, Cintas, Pascal, Tack, Ivan, Cointault, Olivier, Rostaing, Lionel, Vargas-Poussou, Rosa, Ribes, David
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2011
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3052226/
https://ncbi.nlm.nih.gov/pubmed/21030577
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.02870310
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