Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3293612 | Gastroenterology | 2011 | 10 Pages |
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.
Keywords
Related Topics
Health Sciences
Medicine and Dentistry
Gastroenterology
Authors
Manoe J. Janssen, Esmé Waanders, René H.M. te Morsche, Ruoyu Xing, Henry B.P.M. Dijkman, Jannes Woudenberg, Joost P.H. Drenth,