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Paper Details

Exome-Based Rare-Variant Analyses in CKD.
J Am Soc Nephrol
37
2019
AHDC1, APOL1, CKD, COL4A3, COL4A4, COL4A5, CPT2, PKD1, PKD2, Xia-Gibbs syndrome, acute renal injury, carnitine palmitoyltransferase, carnitine palmitoyltransferase II, carnitine palmitoyltransferase II deficiency, causal genes, disease-associated genes, intellectual disability, rare variants, rhabdomyolysis
Author NameAffiliation
Gundula Povysil
Gundula PovysilInstitute for Genomic Medicine, Columbia University Medical Center
Maddalena MarasaColumbia University
Krzysztof KirylukColumbia University
Krzysztof KirylukColumbia University
Andrew S AllenInstitute for Genomic Medicine, Columbia University Medical Center
Andrew S AllenDuke University
David B Goldstein
David B GoldsteinInstitute for Genomic Medicine, Columbia University Medical Center
David B Goldstein
David B Goldstein
David B Goldstein
David B GoldsteinInstitute for Genomic Medicine, Columbia University Medical Center
Ali G GharaviColumbia University
Ali G GharaviInstitute for Genomic Medicine, Columbia University Medical Center
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