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Gianluca Caridi,Abdelbasset Maout,Reha Artan,Monica Campagnoli,Francesca Lugani,Mohamed El Amine Abada,Ersin Sayar,Monica Galliano,Lorenzo Minchiotti 대한진단검사의학회 2018 Annals of Laboratory Medicine Vol.38 No.2
Dear Editor, Congenital analbuminemia (CAA; OMIM # 616000) is a rare autosomal recessive disorder characterized by the complete absence (or extremely low level) of serum albumin (ALB), and is usually diagnosed by serum protein electrophoresis [1]. Since different clinical conditions can result in hypoalbuminemia, mutation analysis of ALB gene is always necessary to confirm the diagnosis of CAA. Since the low ALB level is partially compensated by an increase of other serum proteins