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Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites.
PMID: 10577936 [PubMed - indexed for MEDLINE]
PMCID: PMC1288392
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Cited by 3 PubMed Central articles
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Genetics of focal segmental glomerulosclerosis.
Woroniecki RP, Kopp JB.
Pediatr Nephrol. 2007 May; 22(5):638-44. Epub 2007 Mar 9.
[Pediatr Nephrol. 2007]
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Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function.
Puffenberger EG, Hu-Lince D, Parod JM, Craig DW, Dobrin SE, Conway AR, Donarum EA, Strauss KA, Dunckley T, Cardenas JF, et al.
Proc Natl Acad Sci U S A. 2004 Aug 10; 101(32):11689-94. Epub 2004 Jul 23.
[Proc Natl Acad Sci U S A. 2004]
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Podocin, a raft-associated component of the glomerular slit diaphragm, interacts with CD2AP and nephrin.
Schwarz K, Simons M, Reiser J, Saleem MA, Faul C, Kriz W, Shaw AS, Holzman LB, Mundel P.
J Clin Invest. 2001 Dec; 108(11):1621-9.
[J Clin Invest. 2001]