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Autosomal dominant polycystic liver disease in a family without polycystic kidney disease associated with a novel missense protein kinase C substrate 80K-H mutation

Polycystic liver disease (PLD) is characterized by the presence of multiple bile duct-derived epithelial cysts scattered in the liver parenchyma. PLD can manifest itself in patients with severe autosomal dominant polycystic kidney disease (ADPKD). Isolated autosomal dominant polycystic liver disease...

詳細記述

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書誌詳細
出版年:World J Gastroenterol
主要な著者: Peces, Ramón, Drenth, Joost PH, te Morsche, Rene HM, González, Pedro, Peces, Carlos
フォーマット: Artigo
言語:Inglês
出版事項: Baishideng Publishing Group Inc 2005
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4727230/
https://ncbi.nlm.nih.gov/pubmed/16437702
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v11.i48.7690
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