Molecular Mechanisms of Isolated Polycystic Liver Diseases

Polycystic liver disease (PLD) is a rare autosomal dominant disorder including two genetically and clinically distinct forms: autosomal dominant polycystic kidney disease (ADPKD) and isolated polycystic liver disease (PCLD). The main manifestation of ADPKD is kidney cysts, while PCLD has predominant...

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Detalles Bibliográficos
Autores principales: Yu, Ziqi, Shen, Xiang, Hu, Chong, Zeng, Jun, Wang, Aiyao, Chen, Jianyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104337/
https://www.ncbi.nlm.nih.gov/pubmed/35571028
http://dx.doi.org/10.3389/fgene.2022.846877

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104337/
https://www.ncbi.nlm.nih.gov/pubmed/35571028
http://dx.doi.org/10.3389/fgene.2022.846877

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