2Loudianos G, Lovicu M, Solieas P, et aL. Delineation of the spectrum of Wilson disease mutations in the Greek population and the identification of six novel mutations[J]. genet Test,2000,4(4) :399-402.
3Tarnacka B,Gromadzka G,Rodo M, et al. Frequency of His1069 Gln and Gly1267 Lys mutations in Polish Wilson's disease population[J].Eur J Neuro1,2000,7(5) :495-498.
4Butler P, McIntyre N, Mistry PK. Molecular diagnosis of Wilson disease[J]. Mol Genet Metab, 2001,72 (3) : 223-230.
5Caca K, Ferenci P, Kuhn HJ, et al. High prevalence of the HI069Q mutation in East German patients with Wilson disease : rapid detection of mutations by limited sequencing and phenotypa-genotype analysis[J] .J Hepatol,2001,35(5) :575-581.
6Loudianos G, Kostic V, Solinas P, et al. Characterization of the molecular defect in the ATP7B gene in Wilson disease patients from Yugoslavia[ J], Genet Test, 2003,7(2) : 107-112.
7Firoeisz G, Lakatos PL, Szalay F, et al. Common mutations of ATP7B in Wilson disease patients from Hungary[J]. Am J Med Genet,2002,108( 1 ) :23-28.