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Nature Clinical Practice Nephrology
Volumn 3, Issue 9, 2007, Pages 472-473
Utility of genetic screening in children with nephrotic syndrome presenting during the first year of life: Commentary
Author keywords

[No Author keywords available]
Indexed keywords

LAMININ GAMMA1; NEPHRIN; NUCLEASE; PODOCIN; WT1 PROTEIN;
EID: 34548145333     PISSN: 17458323     EISSN: 17458331     Source Type: Journal    
DOI: 10.1038/ncpneph0560     Document Type: Note
Times cited : (2)
References (5)
  • 1
    • 0032015551 scopus 로고    scopus 로고
    • Positionally cloned gene for a novel glomerular protein - nephrin - is mutated in congenital nephrotic syndrome
    • Kestila M et al. (1998) Positionally cloned gene for a novel glomerular protein - nephrin - is mutated in congenital nephrotic syndrome. Mol Cell 1: 575-582
    • (1998) Mol Cell , vol.1 , pp. 575-582
    • Kestila, M.1
  • 2
    • 8844274003 scopus 로고    scopus 로고
    • Genetic forms of nephrotic syndrome
    • Niaudet P (2004) Genetic forms of nephrotic syndrome. Pediatr Nephrol 19: 1313-1318
    • (2004) Pediatr Nephrol , vol.19 , pp. 1313-1318
    • Niaudet, P.1
  • 3
    • 8844251405 scopus 로고    scopus 로고
    • No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations
    • Schultheiss M et al. (2004) No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations. Pediatr Nephrol 19: 1340-1348
    • (2004) Pediatr Nephrol , vol.19 , pp. 1340-1348
    • Schultheiss, M.1
  • 4
    • 8444221929 scopus 로고    scopus 로고
    • Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
    • Zenker M et al. (2004) Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities. Hum Mol Genet 13: 2625-2632
    • (2004) Hum Mol Genet , vol.13 , pp. 2625-2632
    • Zenker, M.1
  • 5
    • 33751531864 scopus 로고    scopus 로고
    • Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
    • Hinkes B et al. (2006) Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible. Nat Genet 38: 1397-1405
    • (2006) Nat Genet , vol.38 , pp. 1397-1405
    • Hinkes, B.1

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.