Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations.

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Title: Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations.
Authors: Vall-Palomar M; Fisiopatologia Renal, Centre D'Investigacions en Bioquímica I Biologia Molecular (CIBBIM), Institut de Recerca Vall D'Hebron (VHIR), Barcelona, Spain., Burballa C; Fisiopatologia Renal, Centre D'Investigacions en Bioquímica I Biologia Molecular (CIBBIM), Institut de Recerca Vall D'Hebron (VHIR), Barcelona, Spain., Claverie-Martín F; Unidad de Investigación, Hospital Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain., Meseguer A; Fisiopatologia Renal, Centre D'Investigacions en Bioquímica I Biologia Molecular (CIBBIM), Institut de Recerca Vall D'Hebron (VHIR), Barcelona, Spain.; Departament de Bioquímica I Biologia Molecular. Unitat de Bioquímica de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.; Red de Investigación Renal (REDINREN), Instituto Carlos III-FEDER, Madrid, Spain., Ariceta G; Fisiopatologia Renal, Centre D'Investigacions en Bioquímica I Biologia Molecular (CIBBIM), Institut de Recerca Vall D'Hebron (VHIR), Barcelona, Spain. gariceta@vhebron.net.; Servicio de Nefrología Pediátrica, Hospital Universitari Vall D'Hebron, 08035, Barcelona, Spain. gariceta@vhebron.net.; Departamento de Pediatría, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain. gariceta@vhebron.net.
Source: Journal of nephrology [J Nephrol] 2021 Dec; Vol. 34 (6), pp. 2053-2062. Date of Electronic Publication: 2021 Apr 30.
Publication Type: Journal Article; Multicenter Study
Journal Info: Publisher: Springer Country of Publication: Italy NLM ID: 9012268 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1724-6059 (Electronic) Linking ISSN: 11218428 NLM ISO Abbreviation: J Nephrol Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1724-6059
DOI:10.1007/s40620-021-01054-6