Focal and segmental glomerulosclerosis

Cellular and Molecular Life Sciences

Volumn 63, Issue 21, 2006, Pages 2506-2511

  Daskalakis, N ^a   Winn, M P ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

ACTN4; Familial focal segmental glomerulosclerosis; Familial nephropathy; Genetics; Hereditary; Kidney; Nephrin; Podocin; TRPC6

Indexed keywords

ALPHA ACTIN; ALPHA ACTININ 4; NEPHRIN; PODOCIN; TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL 6; TRANSIENT RECEPTOR POTENTIAL CHANNEL; UNCLASSIFIED DRUG;

AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; CONGENITAL NEPHROTIC SYNDROME; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; FOCAL GLOMERULONEPHRITIS; FOCAL SEGMENTAL GLOMERULONEPHRITIS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC DISORDER; GENETIC SCREENING; HUMAN; HUMAN GENOME; KIDNEY FAILURE; NEPHROTIC SYNDROME; NONHUMAN; PATHOGENESIS; RECURRENT DISEASE; REVIEW; STEROID RESISTANCE NEPHROTIC SYNDROME;

GENOME, HUMAN; GLOMERULOSCLEROSIS, FOCAL SEGMENTAL; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MEMBRANE PROTEINS; MUTATION; TRPV CATION CHANNELS;

EID: 33750887047     PISSN: 1420682X     EISSN: 15691632     Source Type: Journal    
DOI: 10.1007/s00018-006-6171-y     Document Type: Review

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