WT-1 and NPHS2 mutation analysis in patients with non-familial steroid-resistant focal-segmental glomerulosclerosis

Clinical Nephrology

Volumn 59, Issue 2, 2003, Pages 143-146

  Lowik M M ^a   Levtchenko, E N ^a   Monnens, L A H ^a   van den Heuvel, L P W J ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Focal segmental glomerulosclerosis; NPHS2 mutation; WT 1 mutation

Indexed keywords

ANGIOTENSIN 2 RECEPTOR ANTAGONIST; CHOLESTEROL; COMPLEMENT COMPONENT C3; COMPLEMENT COMPONENT C4; CREATININE; CYCLOSPORIN A; ENALAPRIL; GENE PRODUCT; MEMBRANE PROTEIN; MYCOPHENOLIC ACID 2 MORPHOLINOETHYL ESTER; PODOCIN; PREDNISONE; PROTEIN WT 1; SERUM ALBUMIN; STEROID; UNCLASSIFIED DRUG;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FOCAL GLOMERULOSCLEROSIS; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; HEMODIALYSIS; HETEROZYGOTE DETECTION; HUMAN; INTRON; LOW DRUG DOSE; MALE; MUTATIONAL ANALYSIS; NEPHRECTOMY; NEPHROTIC SYNDROME; NUCLEOTIDE SEQUENCE; PROGNOSIS; SCHOOL CHILD; TREATMENT PLANNING; URTICARIA;

EID: 0037323347     PISSN: 03010430     EISSN: None     Source Type: Journal    
DOI: 10.5414/CNP59143     Document Type: Article

References (13)

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