Identifizierung und Charakterisierung neuer Interaktionspartner von Fibrocystin, dem Protein der autosomal rezessiven polyzystischen Nierenerkrankung (ARPKD)

Autor: Venghaus, Andreas

Publikováno v: Aachen : Publikationsserver der RWTH Aachen University 122 Bl. : Ill., graph. Darst. (2013). = Aachen, Techn. Hochsch., Diss., 2013

Autosomal recessive polycystic kidney disease (ARPKD) is a monogenetic hereditary disease during the childhood with an incidence of 1:20.000. It is caused by mutations in the gene PKHD1. Phenotypically it is characterized in mainly small-cystic kidne

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______791::672e9f4b4770624c2e1201c13065a7e3
https://publications.rwth-aachen.de/record/229334