Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia
Background/Aim. Wilson’s disease (WD) is an autosomal-recessive disorder which is characterized with a marked clinical heterogeneity. The gene responsible for WD is located in 13q14.3 chromosome, contains 21 exons and codes for copper specific transporting P-type adenosinetriphosphatase (ATPase)...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Military Health Department, Ministry of Defance, Serbia
2013-01-01
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Series: | Vojnosanitetski Pregled |
Subjects: | |
Online Access: | http://www.doiserbia.nb.rs/img/doi/0042-8450/2013/0042-84501305457T.pdf |