2Fine JM, Marneux M, Rochu D. Human albumin genetics variants:Am attempt at a classification of European allotype. Am J Hum Genet, 1987 ,40 :278-286.
3Brennan SO, Aroci K, Madison J, et al. Hypermutability of CpG Dinucleotide in the propeptide-encoding sequence of the human albumin gene. Proc Natl Acad Sci U S A,1990,87:3909-3913.
4Watkins S, Madison J, Galliano M, et al. A nucleotide insertion and frameshift cause analbuminemia in an Italian family. Proc Natl Acad Sci USA, 1994,91:2275-2279.
5张秀祥 蔡建霖 石志忠.一个患者家族性血蛋白异常甲状腺素过高的华人家庭的病例[J].Hong Kong Ned,2003,9:464-467.
6Galliano M, Campagnoli M, Rossi A, et al. Molecular diagnosis of analbuminemia: A novel mutation identified in two amerindian and two turkish families. Clin Chem, 2002, 48 (6pt1) : 844-849.
