Journal article
Exome sequencing of Saudi Arabian patients with ADPKD
Abstract
Purpose: Autosomal dominant polycystic kidney disease (ADPKD) is characterized by progressive development of kidney cysts and enlargement and dysfunction of the kidneys. The Consortium of Radiologic Imaging Studies of the Polycystic Kidney Disease (CRISP) cohort revealed that 89.1% had either a PKD1 or PKD2 mutation. Of the CRISP patients with a genetic cause detected, mutations in PKD1 accounted for 85%, while mutations in the PKD2 accounted …
Authors
Al-Muhanna FA; Al-Rubaish AM; Vatte C; Mohiuddin SS; Cyrus C; Ahmad A; Akhtar MS; Albezra MA; Alali RA; Almuhanna AF
Journal
Renal Failure, Vol. 41, No. 1, pp. 842–849
Publisher
Taylor & Francis
Publication Date
January 2019
DOI
10.1080/0886022x.2019.1655453
ISSN
0886-022X
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AdultAgedArabsCalcium ChannelsCase-Control StudiesCystic Fibrosis Transmembrane Conductance RegulatorDNA Mutational AnalysisEpidermal Growth FactorExonsFemaleHumansMaleMiddle AgedMutation, MissensePolycystic Kidney, Autosomal DominantReceptors, Cell SurfaceSaudi ArabiaTRPP Cation ChannelsTomography, X-Ray ComputedTuberous Sclerosis Complex 2 ProteinExome Sequencing