Extensive mutational analysis of PRKCSH
β
EsmΓ© Waanders; RenΓ© H.M. te Morsche; Rob A. de Man; Jan B.M.J. Jansen; Joost P.H
π
Article
π
2006
π
John Wiley and Sons
π
English
β 343 KB
## Communicated by Claude Ferec Autosomal dominant polycystic liver disease (PCLD) is characterized by progressive development of multiple (>20) liver cysts. Two separate genes, PRKCSH and SEC63, have been identified to cause familial PCLD. We designed this study with two goals: to assess the rela