GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome.

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2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome.

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GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome.

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GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome.

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GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome.

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GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome.

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GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome.

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P1476

GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome

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P2093

Hae Il Cheong

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Hee Gyung Kang

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P2860

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene

The International HapMap Project

Common variation in GPC5 is associated with acquired nephrotic syndrome

ACE I/D gene polymorphism can't predict the steroid responsiveness in Asian children with idiopathic nephrotic syndrome: a meta-analysis

Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations.

A case of unfulfilled expectations. Cytokines in idiopathic minimal lesion nephrotic syndrome.

Genomewide association between GLCCI1 and response to glucocorticoid therapy in asthma.

Urine proteomic profiling to identify biomarkers of steroid resistance in pediatric nephrotic syndrome.

Management of childhood onset nephrotic syndrome.

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s00467-012-2197-6

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1595-1599

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scholarly article

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10.1007/S00467-012-2197-6

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Johannes Schlöndorff

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2012-06-04T00:00:00Z

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225095164

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22660954

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single-nucleotide polymorphism

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3408784

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