A whole genome SNP genotyping by DNA microarray and candidate gene association study for kidney stone disease
about
The genetic framework for development of nephrolithiasis.Loss-of-function mutations of SCN10A encoding NaV1.8 α subunit of voltage-gated sodium channel in patients with human kidney stone disease.The Long Pentraxin PTX3 Is an Endogenous Inhibitor of Hyperoxaluria-Related Nephrocalcinosis and Chronic Kidney Disease
P2860
A whole genome SNP genotyping by DNA microarray and candidate gene association study for kidney stone disease
description
2014 nî lūn-bûn
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2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին 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
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
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name
A whole genome SNP genotyping ...... study for kidney stone disease
@ast
A whole genome SNP genotyping ...... study for kidney stone disease
@en
type
label
A whole genome SNP genotyping ...... study for kidney stone disease
@ast
A whole genome SNP genotyping ...... study for kidney stone disease
@en
prefLabel
A whole genome SNP genotyping ...... study for kidney stone disease
@ast
A whole genome SNP genotyping ...... study for kidney stone disease
@en
P2093
P2860
P356
P1433
P1476
A whole genome SNP genotyping ...... study for kidney stone disease
@en
P2093
Choochai Nettuwakul
Duangporn Chuawattana
Nanyawan Rungroj
Nirinya Sudtachat
Nunghathai Sawasdee
Oranud Praditsap
Pa-Thai Yenchitsomanus
Suchai Sritippayawan
P2860
P2888
P356
10.1186/1471-2350-15-50
P577
2014-05-02T00:00:00Z