Authors
Ying‐Cai Tan, Jon D Blumenfeld, Raluca Anghel, Stephanie Donahue, Rimma Belenkaya, Marina Balina, Thomas Parker, Daniel Levine, Debra GB Leonard, Hanna Rennert
Publication date
2009/2
Journal
Human mutation
Volume
30
Issue
2
Pages
264-273
Publisher
Wiley Subscription Services, Inc., A Wiley Company
Description
Genetic testing of PKD1 and PKD2 is useful for diagnosis and prognosis of autosomal dominant polycystic kidney disease (ADPKD), particularly in asymptomatic individuals or those without a family history. PKD1 testing is complicated by the large transcript size, complexity of the gene region, and the extent of gene variations. A molecular assay was developed using Transgenomic's SURVEYOR Nuclease and WAVE Nucleic Acid High Sensitivity Fragment Analysis System to screen for PKD1 and PKD2 variants, followed by sequencing of variant gene segments, thereby reducing the sequencing reactions by 80%. This method was compared to complete DNA sequencing performed by a reference laboratory for 25 ADPKD patients from 22 families. The pathogenic potential of gene variations of unknown significance was examined by evolutionary comparison, effects of amino acid substitutions on protein structure …
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