Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthood [1]

Kidney International

Volumn 64, Issue 1, 2003, Pages 365-

  Caridi, Gianluca ^b   Bertelli, Roberta ^b   Scolari, Francesco ^b   Sanna Cherchi, Simone ^b   Di Duca, Marco ^b   Ghiggeri, Gian Marco ^a  

^a G GASLINI INSTITUTE   (Italy)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SUBSTITUTION; CLINICAL FEATURE; EXON; GENETIC CONSERVATION; GLOMERULOSCLEROSIS; HUMAN; KIDNEY BIOPSY; KIDNEY FAILURE; KIDNEY TRANSPLANTATION; LETTER; MAJOR CLINICAL STUDY; NEPHROTIC SYNDROME; POINT MUTATION; PRIORITY JOURNAL; PROTEINURIA; RECURRENT DISEASE;

EID: 0037792031     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1755.2003.00084.x     Document Type: Letter

References (3)

1. BOUTE N, GRIBOUVAL O, ROSELLI S, et al: NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome. Nat Genet 24:349-354, 2000
2. CARIDI G, BERTELLI R, CARREA A, et al: Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis. J Am Soc Nephrol 12:2742-2746, 2001
3. CARIDI G, BERTELLI R, DI DUCA M, et al: Broadening the spectrum of diseases related to podocin mutations. J Am Soc Nephrol, 2003