Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS

Pediatric Nephrology

Volumn 24, Issue 2, 2009, Pages 281-285

  Gbadegesin, Rasheed ^a   Bartkowiak, Bartlomiej ^a   Lavin, Peter J ^a   Mukerji, Nirvan ^a   Wu, Guanghong ^a   Bowling, Brandy ^a   Eckel, Jason ^a   Damodaran, Tirupapuliyur ^a   Winn, Michelle P ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Familial focal segmental glomerulosclerosis; Familial nephropathy; FSGS; Genetics; Hereditary; PLCE1 mutation

Indexed keywords

PHOSPHOLIPASE C; PHOSPHOLIPASE C EPSILON1; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CONTROLLED STUDY; FOCAL GLOMERULOSCLEROSIS; GENETIC ANALYSIS; HOMOZYGOSITY; HUMAN; KIDNEY FAILURE; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; NEPHROTIC SYNDROME; PEDIGREE ANALYSIS; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGE OF ONSET; COHORT STUDIES; FAMILY HEALTH; GLOMERULOSCLEROSIS, FOCAL SEGMENTAL; HOMOZYGOTE; HUMANS; MIDDLE AGED; MUTATION, MISSENSE; PHOSPHOINOSITIDE PHOSPHOLIPASE C; POLYMORPHISM, SINGLE NUCLEOTIDE; YOUNG ADULT;

EID: 58149094460     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-008-1025-5     Document Type: Article

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