References
1. Kim YH, Lee YW, Jeon BR, Lee YK, Shin HB, Kang DH, et al. Clinical characteristics and ALB gene mutation analysis of Korean patients with bisalbuminemia. Korean J Lab Med 2010;30:307–11.Search in Google Scholar
2. Jaeggi-Groisman SE, Byland C, Gerber H. Improved sensitivity of capillary electrophoresis for detection of bisalbuminemia. Clin Chem 2000;46:882–3.Search in Google Scholar
3. Hoang MP, Baskin LB, Wians FH. Bisalbuminuria in an adult with bisalbuminemia and nephrotic syndrome. Clin Chim Acta 1999;284:101–7.Search in Google Scholar
4. Chhabra S, Bansal F, Saikia B, Minz RW. Bisalbuminemia: a rarely encountered protein anomaly. J Lab Physicians 2013;5:145–6.Search in Google Scholar
5. Kalambokis G, Kitsanou M, Kalogera C, Kolios G, Seferiadis K, Tsianos E. Inherited bisalbuminemia with benign monoclonal gammopathy detected by capillary but not agarose gel electrophoresis. Clin Chem 2002;48:2076–7.Search in Google Scholar
6. Kragh-Hansen U, Brennan SO, Galliano M, Sugita O. Binding of warfarin, salicylate, and diazepam to genetic variants of human serum albumin with known mutations. Mol Pharmacol 1990;37:238–42.Search in Google Scholar
7. Kragh-Hansen U, Minchiotti L, Brennan SO, Sugita O. Hormone binding to natural mutants of human serum albumin. Eur J Biochem 1990;193:169–74.Search in Google Scholar
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