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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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Detalhes bibliográficos
Publicado no:Kidney360
Main Authors: Besse, Whitney, Roosendaal, Charlotte, Tuccillo, Luigi, Ghosh Roy, Sounak, Gallagher, Anna-Rachel, Somlo, Stefan
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2020
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Acesso em linha: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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