NPHS2 mutations account for only 15% of nephrotic syndrome cases.

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NPHS2 Mutations: A Closer Look to Latin American Countries.Whole exome sequencing in three families segregating a pediatric case of sarcoidosis.

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NPHS2 mutations account for only 15% of nephrotic syndrome cases.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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2015年论文

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2015年论文

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NPHS2 mutations account for only 15% of nephrotic syndrome cases.

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NPHS2 mutations account for only 15% of nephrotic syndrome cases.

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type

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label

NPHS2 mutations account for only 15% of nephrotic syndrome cases.

@ast

NPHS2 mutations account for only 15% of nephrotic syndrome cases.

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prefLabel

NPHS2 mutations account for only 15% of nephrotic syndrome cases.

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NPHS2 mutations account for only 15% of nephrotic syndrome cases.

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P1476

NPHS2 mutations account for only 15% of nephrotic syndrome cases

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P2093

Anna Cristina G B Lutaif

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Cristiane S C Piveta

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Marcela L Souza

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Maricilda P De Mello

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Suéllen R de Souza

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Taciane B Henriques

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P2860

Predicting deleterious amino acid substitutions

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations

NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

Association of an anatomo-pathological syndrome of male pseudohermaphroditism, Wilms' tumor, parenchymatous nephropathy and XX/XY mosaicism

P2888

s12881-015-0231-9

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scholarly article

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10.1186/S12881-015-0231-9

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Gil Guerra-Junior

Mara Sanches Guaragna

A T Maciel-Guerra

Vera Maria Santoro Belangero

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2015-09-29T00:00:00Z

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282355642

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26420286

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4589073

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NPHS2 mutations account for only 15% of nephrotic syndrome cases.

about

P2860

P2860

NPHS2 mutations account for only 15% of nephrotic syndrome cases.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P50

P577

P5875

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P478

P50

P577

P5875

P6179

P698

P932