Open AccessMO036: Detection of copy number variations by single-nucleotide-polymorphism array in patients with end-stage renal disease of unknown etiology
Author(s) -
Jeff Granhøj,
Katja Venborg Pedersen,
Henrik Birn,
Dorte L. Lildballe,
Marit E. Jørgensen,
Jesper Graakjær,
Maria Rasmussen
Publication year - 2022
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/gfac062.017
Subject(s) - medicine , kidney disease , end stage renal disease , copy number variation , penetrance , etiology , single nucleotide polymorphism , nephrology , snp array , disease , snp , kidney , pathology , bioinformatics , genetics , genotype , biology , genome , phenotype , gene
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