Case Report
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World J Gastroenterol. Dec 28, 2005; 11(48): 7690-7693
Published online Dec 28, 2005. doi: 10.3748/wjg.v11.i48.7690
Autosomal dominant polycystic liver disease in a family without polycystic kidney disease associated with a novel missense protein kinase C substrate 80K-H mutation
Ramón Peces, Joost PH Drenth, Rene HM te Morsche, Pedro González, Carlos Peces
Ramón Peces, Section of Nephrology, Hospital General La Mancha-Centro, Alcázar de San Juan, Ciudad Real and Service of Nephrology, Hospital Universitario La Paz, Madrid, Spain
Joost PH Drenth, Rene HM te Morsche, Department of Medicine, Division of Gastroenterology and Hepatology, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands
Pedro González, Section of Digestive Hospital General La Mancha-Centro, Alcázar de San Juan, Ciudad Real, Spain
Carlos Peces, Computer Science Superior School, Castilla La Mancha University and Technology Area of the Castilla La Mancha Health Service (SESCAM), Ciudad Real, Spain
Author contributions: All authors contributed equally to the work.
Supported by a grant from the Instituto de Ciencias de la Salud, Consejería de Sanidad de Castilla La Mancha (Grant EQ03016). Joost PH Drenth is a recipient of a NOW-VIDI grant
Correspondence to: Dr Ramón Peces, Servicio de Nefrología, Hospital Universitario La Paz, Paseo de la Castellana 261, 28046 Madrid, Spain. cpeces@varnet.com
Telephone: +34-917277224 Fax: +34-917277133
Received: December 15, 2004
Revised: June 10, 2005
Accepted: June 16, 2005
Published online: December 28, 2005
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