Synergistic Genetic Interactions between Pkhd1 and Pkd1 Result in an ARPKD-Like Phenotype in Murine Models

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Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts.

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LETTER TO JMG Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts

A utosomal recessive polycystic kidney disease (ARPKD; MIM 263200) is an important childhood nephropathy, occurring in 1 in 20 000 live births. The clinical phenotype is dominated by dilatation of the renal collecting ducts, biliary dysgenesis, and portal tract fibrosis. Affected children often present in utero with enlarged, echogenic kidneys, as well as oligohydramnios secondary to poor urine...

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ژورنال

عنوان ژورنال: Journal of the American Society of Nephrology

سال: 2019

ISSN: 1046-6673,1533-3450

DOI: 10.1681/asn.2019020150