Claudin-19 mutations and clinical phenotype in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
about
Identification of the first large deletion in the CLDN16 gene in a patient with FHHNC and late-onset of chronic kidney disease: case report.Clinical utility gene card for: Familial hypomagnesemia with hypercalciuria and nephrocalcinosis with/without severe ocular involvement.The claudin family of proteins in human malignancy: a clinical perspectiveDietary magnesium and genetic interactions in diabetes and related risk factors: a brief overview of current knowledge.Inherited disorders of renal hypomagnesaemia.Ways of calcium reabsorption in the kidney.Claudin-4 is required for AMPK-modulated paracellular permeability in submandibular gland cells.Inherited and acquired disorders of magnesium homeostasis.Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations.First report of a novel missense CLDN19 mutations causing familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a Chinese family.Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: variable phenotypic expression in three affected sisters from Mexican ancestry.Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis: clinical and molecular characteristics.Novel Aspects of Renal Magnesium Homeostasis.Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
P2860
Q35681297-D4E42608-8850-4AAE-A250-5E0AEB8C1599Q36695106-19A42605-0251-433C-9FDC-7C36F6E648CBQ37302556-3884C22E-DF5F-4CBD-A2AA-4E71D183498FQ37420495-56CC7AFA-8C55-4D7E-9587-12E26D90F288Q38244120-A70ED25C-6C67-4078-BB99-90758EF35C54Q38786641-D3EC587C-F381-4495-8E11-24215C68C244Q38928944-D6D1C5E2-BA18-4A13-AE05-A2ADBF8C1BC2Q39025913-D660FBF6-B2F4-4AB5-8B13-70FE7431F834Q39484986-81D1AFEF-6A7C-45C9-A73B-67D78FD85C87Q41630174-3B85A066-F1E9-4F5A-BAC0-A0B8D6E6CD25Q41679190-5AA75FB5-754F-4F1E-B2BA-FE5FF1577E7CQ41996768-FB259E05-F3EE-4DE3-86B7-4D6B87CED19EQ52568181-AE25860F-5083-462A-817E-5A90E023DB70Q54184511-3A5B2D80-B4E0-493B-9255-AB40DE74161F
P2860
Claudin-19 mutations and clinical phenotype in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Claudin-19 mutations and clini ...... alciuria and nephrocalcinosis.
@ast
Claudin-19 mutations and clini ...... alciuria and nephrocalcinosis.
@en
Claudin-19 mutations and clini ...... alciuria and nephrocalcinosis.
@nl
type
label
Claudin-19 mutations and clini ...... alciuria and nephrocalcinosis.
@ast
Claudin-19 mutations and clini ...... alciuria and nephrocalcinosis.
@en
Claudin-19 mutations and clini ...... alciuria and nephrocalcinosis.
@nl
prefLabel
Claudin-19 mutations and clini ...... alciuria and nephrocalcinosis.
@ast
Claudin-19 mutations and clini ...... alciuria and nephrocalcinosis.
@en
Claudin-19 mutations and clini ...... alciuria and nephrocalcinosis.
@nl
P2093
P2860
P1433
P1476
Claudin-19 mutations and clini ...... alciuria and nephrocalcinosis.
@en
P2093
Africa Avila
Ana Sanchez
Cesar Loris
Elena García-Martinez
Elizabeth Córdoba-Lanus
Fernando Santos
Gema Ariceta
Hilaria González-Acosta
Inmaculada Nadal
Laura Espinosa
P2860
P304
P356
10.1371/JOURNAL.PONE.0053151
P407
P577
2013-01-03T00:00:00Z