Segregation of hematuria in thin basement membrane disease with haplotypes at the loci for Alport syndrome

Kidney International

Volumn 59, Issue 5, 2001, Pages 1670-1676

  Buzza, Mark ^a,b,c   Wilson, Diane ^a,b,c   Savige, Judy ^a,b,c  

^a UNIVERSITY OF MELBOURNE   (Australia)

^b AUSTIN HEALTH   (Australia)

^c BOX HILL HOSPITAL   (Australia)

Author keywords

Benign familial hematuria; Collagen chains; Gene mutation; Hematuria; Inherited disease

Indexed keywords

ALPORT SYNDROME; ARTICLE; GENE LOCUS; GLOMERULUS BASEMENT MEMBRANE; HAPLOTYPE; HEMATURIA; HUMAN; HUMAN CELL; PRIORITY JOURNAL; X CHROMOSOME LINKAGE;

EID: 0035046418     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1755.2001.0590051670.x     Document Type: Article

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