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Niemann-Pick type C disease (NPC) is a rare, recessive, fatal, lipid storage disorder caused by mutations in NPC1 or NPC2 genes. NPC1/NPC2 code for cholesterol transport proteins. Their dysfunction leads to accumulation of free cholesterol and other
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::dea7dd3728879d39fc3c5f68b9fcaded
https://www.bib.irb.hr/1175484
https://www.bib.irb.hr/1175484
Autor:
Popic J; Department of Radiology, University Hospital Merkur, School of Medicine, University of Zagreb, Zagreb 10000, Croatia., Tipuric S; Department of Family Medicine, Health Center Zagreb-East, Zagreb 10000, Croatia., Balen I; Department of Gastroenterology and Endocrinology, General Hospital Slavonski brod 'Dr. Josip Bencevic', Slavonski Brod 35000, Croatia., Mrzljak A; Department of Medicine, Merkur University Hospital, School of Medicine, University of Zagreb, Zagreb 10000, Croatia. anna.mrzljak@gmail.com.
Publikováno v:
World journal of gastrointestinal endoscopy [World J Gastrointest Endosc] 2021 Mar 16; Vol. 13 (3), pp. 72-81.
