Open AccessCorrection: Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
Author(s) -
Félix Claverie-Martı́n,
Víctor GarcíaNieto,
C Loris,
Gema Ariceta,
Inmaculada Nadal,
Laura Espinosa,
Ángeles Fernández-Maseda,
Montserrat AntónGamero,
África Avila,
Álvaro Madrid,
Hilaria González-Acosta,
Elizabeth Córdoba-Lanús,
Fernando Santos,
Marta Gil-Calvo,
Mar Espino,
Elena GarcíaMartínez,
Ana María Hernández Sánchez,
Rafael Muley
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/annotation/25732fb0-ae38-40f6-b8c6-eb4ba94ac996
Subject(s) - nephrocalcinosis , hypercalciuria , hypomagnesemia , claudin , medicine , phenotype , hypophagia , correct name , genetics , endocrinology , bioinformatics , pediatrics , biology , calcium , kidney , chemistry , gene , paleontology , organic chemistry , tight junction , magnesium , hypothalamus