Rare genetic causes of complex kidney and urological diseases

Although often considered a single-entity, chronic kidney disease (CKD) comprises many pathophysiologically distinct disorders that result in persistently abnormal kidney structure and/or function, and encompass both monogenic and polygenic aetiologies. Rare inherited forms of CKD frequently span di...

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Veröffentlicht in:	Nature reviews. Nephrology 2020-11, Vol.16 (11), p.641-656
Hauptverfasser:	Groopman, Emily E., Povysil, Gundula, Goldstein, David. B., Gharavi, Ali G.
Format:	Artikel
Sprache:	eng
Schlagworte:	631/208/212/2166 692/4022/1585/104 Care and treatment Chromosome Mapping Development and progression Diabetes Etiology Genetic aspects Genetic research Genetic susceptibility Genomes Genotype Health aspects High-Throughput Nucleotide Sequencing Humans Kidney diseases Medical research Medicine Medicine & Public Health Medicine, Experimental Mutation Nephrology Pathogenesis Phenotype Precision Medicine Renal Insufficiency, Chronic - genetics Renal Insufficiency, Chronic - therapy Review Article Surgeons Urologic Diseases - genetics Urologic Diseases - therapy
Online-Zugang:	Volltext
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