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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Publicado en:Kidney360
Autores principales: Besse, Whitney, Roosendaal, Charlotte, Tuccillo, Luigi, Ghosh Roy, Sounak, Gallagher, Anna-Rachel, Somlo, Stefan
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society of Nephrology 2020
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Original Investigations
Acceso en línea: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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