Secondary and tertiary structure modeling reveals effects of novel mutations in polycystic liver disease genes PRKCSH and SEC63 Waanders E, Venselaar H, te Morsche RHM, de Koning DB, Kamath PS, Torres VE, Somlo S, Drenth JPH. Secondary and tertiary structure modeling reveals effects of novel mutations in polycystic liver disease genes PRKCSH and SEC63
BACKGROUND & AIMS: Heterozygous germline mutations in PRKCSH cause autosomal dominant polycystic liv...
Polycystic liver disease (PCLD, MIM 174050) is a dominantly inherited condition characterised by the...
Contains fulltext : 89364.pdf (publisher's version ) (Closed access)Autosomal domi...
Contains fulltext : 89294.pdf (publisher's version ) (Closed access)Polycystic liv...
Contains fulltext : 49901.pdf (publisher's version ) (Closed access)Autosomal domi...
Autosomal dominant polycystic liver disease (PCLD) is characterized by progressive development of mu...
Polycystic liver disease (PCLD) is characterized by a severe enlarged liver containing numerous cyst...
Contains fulltext : 108556.pdf (publisher's version ) (Open Access)Polycystic live...
Polycystic liver disease (PCLD) is an autosomal dominant disorder characterised by multiple fluid fi...
Contains fulltext : 57602.pdf (publisher's version ) (Closed access)Mutations in p...
Autosomal-dominant polycystic liver disease (PCLD) is a rare disorder that is characterized by the p...
Item does not contain fulltextPURPOSE OF REVIEW: This review provides an outline of the most recent ...
Polycystic liver diseases are genetic disorders characterized by progressive bile duct dilatation an...
Polycystic liver disease (PCLD, OMIM 174050) is a dominantly inherited condition characterized by th...
Contains fulltext : 145297.pdf (publisher's version ) (Open Access)16 november 201...
BACKGROUND & AIMS: Heterozygous germline mutations in PRKCSH cause autosomal dominant polycystic liv...
Polycystic liver disease (PCLD, MIM 174050) is a dominantly inherited condition characterised by the...
Contains fulltext : 89364.pdf (publisher's version ) (Closed access)Autosomal domi...
Contains fulltext : 89294.pdf (publisher's version ) (Closed access)Polycystic liv...
Contains fulltext : 49901.pdf (publisher's version ) (Closed access)Autosomal domi...
Autosomal dominant polycystic liver disease (PCLD) is characterized by progressive development of mu...
Polycystic liver disease (PCLD) is characterized by a severe enlarged liver containing numerous cyst...
Contains fulltext : 108556.pdf (publisher's version ) (Open Access)Polycystic live...
Polycystic liver disease (PCLD) is an autosomal dominant disorder characterised by multiple fluid fi...
Contains fulltext : 57602.pdf (publisher's version ) (Closed access)Mutations in p...
Autosomal-dominant polycystic liver disease (PCLD) is a rare disorder that is characterized by the p...
Item does not contain fulltextPURPOSE OF REVIEW: This review provides an outline of the most recent ...
Polycystic liver diseases are genetic disorders characterized by progressive bile duct dilatation an...
Polycystic liver disease (PCLD, OMIM 174050) is a dominantly inherited condition characterized by th...
Contains fulltext : 145297.pdf (publisher's version ) (Open Access)16 november 201...
BACKGROUND & AIMS: Heterozygous germline mutations in PRKCSH cause autosomal dominant polycystic liv...
Polycystic liver disease (PCLD, MIM 174050) is a dominantly inherited condition characterised by the...
Contains fulltext : 89364.pdf (publisher's version ) (Closed access)Autosomal domi...