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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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: The American Society of Human Genetics 2000
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC1287938/
https://ncbi.nlm.nih.gov/pubmed/11047756
Tagiau: Ychwanegu Tag
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