Exome sequencing identifies a novel homozygous mutation in the phosphate transporter SLC34A1 in hypophosphatemia and nephrocalcinosis
about
Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile HypercalcemiaThe Envy of Scholars: Applying the Lessons of the Framingham Heart Study to the Prevention of Chronic Kidney DiseasePTH and Vitamin D.Loss of function of NaPiIIa causes nephrocalcinosis and possibly kidney insufficiency.The intestinal phosphate transporter NaPi-IIb (Slc34a2) is required to protect bone during dietary phosphate restriction.Renal phosphate handling and inherited disorders of phosphate reabsorption: an update.
P2860
Exome sequencing identifies a novel homozygous mutation in the phosphate transporter SLC34A1 in hypophosphatemia and nephrocalcinosis
description
2014 nî lūn-bûn
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2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հուլիսին հրատարակված գիտական հոդված
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2014年の論文
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2014年論文
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2014年論文
@zh-hant
2014年論文
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2014年論文
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2014年論文
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2014年论文
@wuu
name
Exome sequencing identifies a ...... sphatemia and nephrocalcinosis
@ast
Exome sequencing identifies a ...... sphatemia and nephrocalcinosis
@en
Exome sequencing identifies a ...... sphatemia and nephrocalcinosis
@nl
type
label
Exome sequencing identifies a ...... sphatemia and nephrocalcinosis
@ast
Exome sequencing identifies a ...... sphatemia and nephrocalcinosis
@en
Exome sequencing identifies a ...... sphatemia and nephrocalcinosis
@nl
prefLabel
Exome sequencing identifies a ...... sphatemia and nephrocalcinosis
@ast
Exome sequencing identifies a ...... sphatemia and nephrocalcinosis
@en
Exome sequencing identifies a ...... sphatemia and nephrocalcinosis
@nl
P2093
P2860
P356
P1476
Exome sequencing identifies a ...... sphatemia and nephrocalcinosis
@en
P2093
Abbhirami Rajagopal
Brendan H Lee
David S Liu
Débora Braslavsky
Florencia Clément
Graciela Vallejo
Hamilton Cassinelli
Ignacio Bergadá
James T Lu
Jose Miguel Liern
P2860
P304
P356
10.1210/JC.2014-1517
P407
P577
2014-07-22T00:00:00Z