Article ID Journal Published Year Pages File Type
3293612 Gastroenterology 2011 10 Pages PDF
Abstract
Among patients with PCLD who have a heterozygous germline mutation in PRKCSH, we found secondary, somatic mutations (second hits) in more than 76% of the liver cyst epithelia. PCLD is recessive at the cellular level, and loss of functional PRKCSH is an important step in cystogenesis.
Related Topics
Health Sciences Medicine and Dentistry Gastroenterology
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