Identification of the First Gene Locus (SSNS1) for Steroid-Sensitive Nephrotic Syndrome on Chromosome 2p - Ruf, Rainer G.; Fuchshuber, Arno; Karle, Stephanie M.; Lemainque, Arnaud; Huck, Kirsten; Wienker, Thomas; Otto, Edgar; Hildebrandt, Friedhelm (Journal of the American Society of Nephrology, 2003)
Keywords: Age of Onset; Biological and medical sciences; Child; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 2; Cloning, Molecular; Female; Genetic Linkage; Genetic Markers; Genome; Glomerulonephritis; Haplotypes; Homozygote; Humans; Infant; Lod Score; Male; Medical sciences; Models, Genetic; Nephrology. Urinary tract diseases; Nephropathies. Renovascular diseases. Renal failure; Nephrotic Syndrome - genetics; Pedigree; Glomerulonephritis; Kidney disease; Human; Urinary system disease; Linkage; Family study; Etiopathogenesis; Nephrotic syndrome; Chromosome 2; Genetic determinism; Loss of heterozygosity; Locus; Child