Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis

Kidney International

Volumn 55, Issue 4, 1999, Pages 1241-1246

  Winn, Michelle P ^a,b,c   Conlon, Peter J ^a,b,c   Lynn, Kelvin L ^a,b,c   Howell, David N ^a,b,c   Gross, Deborah A ^a,b,c   Rogala, Allison R ^a,b,c   Smith, Anne H ^a,b,c   Graham, Felicia L ^a,b,c   Bembe, MaryLou ^a,b,c   Quarles, L Daryl ^a,b,c   Pericak Vance, Margaret A ^a,b,c   Vance, Jeffery M ^a,b,c  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b BEAUMONT HOSPITAL   (Ireland)

^c CHRISTCHURCH HOSPITAL   (New Zealand)

Author keywords

Familial nephropathy; Glomerular sclerosis; Heredity; Progressive renal disease; Tuft collapse

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 19Q; CLINICAL FEATURE; CONTROLLED STUDY; DNA DETERMINATION; FAMILIAL DISEASE; FAMILY STUDY; FEMALE; GENETIC LINKAGE; GENETIC SCREENING; GENETIC VARIABILITY; GLOMERULOSCLEROSIS; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; PEDIGREE ANALYSIS; PRIORITY JOURNAL;

EID: 0032922319     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1755.1999.00384.x     Document Type: Article

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