Adult Inactivation of the Recessive Polycystic Kidney Disease Gene Causes Polycystic Liver Disease

BACKGROUND: A major difference between autosomal recessive polycystic kidney disease (ARPKD) and autosomal dominant polycystic kidney disease (ADPKD) lies in the pattern of inheritance, and the resultant timing and focality of cyst formation. In both diseases, cysts form in the kidney and liver as a...

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Bibliografiska uppgifter
I publikationen:Kidney360
Huvudupphovsmän: Besse, Whitney, Roosendaal, Charlotte, Tuccillo, Luigi, Ghosh Roy, Sounak, Gallagher, Anna-Rachel, Somlo, Stefan
Materialtyp: Artigo
Språk:Inglês
Publicerad: American Society of Nephrology 2020
Ämnen:
Original Investigations
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7861569/
https://ncbi.nlm.nih.gov/pubmed/33554127
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.34067/KID.0002522020
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