Identification of a Locus for Autosomal Dominant Polycystic Liver Disease, on Chromosome 19p13.2-13.1

Polycystic liver disease (PCLD) is characterized by the growth of fluid-filled cysts of biliary epithelial origin in the liver. Although the disease is often asymptomatic, it can, when severe, lead to complications requiring surgical therapy. PCLD is most often associated with autosomal dominant pol...

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Detalhes bibliográficos
Main Authors: Reynolds, David M., Falk, Cathy T., Li, Airong, King, Bernard F., Kamath, Patrick S., Huston III, John, Shub, Clarence, Iglesias, Diana M., Martin, Rodolfo S., Pirson, Yves, Torres, Vicente E., Somlo, Stefan
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2000
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1287938/
https://ncbi.nlm.nih.gov/pubmed/11047756
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