Laparoscopische cholecystectomie in dagbehandeling; implementatie van een richtlijn voor klinisch handelen

From gene to disease; α1-antitrypsin deficiency. – Alpha-1antitrypsin (α1-AT) deficiency is an autosomal, recessive hereditary disorder that is associated with the development of pulmonary emphysema and liver disease. The most common mutant leading to the deficiency is the Z mutant. This results