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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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| Publicado no: | Kidney360 |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Nephrology
2020
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| Assuntos: | |
| 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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