Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adults.

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Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adults.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

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2018年學術文章

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2018年學術文章

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name

Clinical and pathological phen ...... glomerulosclerosis in adults.

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Clinical and pathological phen ...... glomerulosclerosis in adults.

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type

Item

label

Clinical and pathological phen ...... glomerulosclerosis in adults.

@en

Clinical and pathological phen ...... glomerulosclerosis in adults.

@nl

prefLabel

Clinical and pathological phen ...... glomerulosclerosis in adults.

@en

Clinical and pathological phen ...... glomerulosclerosis in adults.

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P1476

Clinical and pathological phen ...... glomerulosclerosis in adults.

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P2093

Fernando C Fervenza

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Gema Fernandez-Juarez

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Ladan Zand

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Nicola Lepori

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Sanjeev Sethi

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P2860

Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS

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

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

Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome

Genetic causes of focal segmental glomerulosclerosis: implications for clinical practice

Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13

Targeted exome sequencing integrated with clinicopathological information reveals novel and rare mutations in atypical, suspected and unknown cases of Alport syndrome or proteinuria

CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS).

P304

179-190

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P31

scholarly article

P356

10.1093/CKJ/SFX143

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P433

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P478

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P577

2018-01-09T00:00:00Z

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P698

29644057

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P932

5888331

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