p. 1−7
2538-4473
Vol.1/No.1
p. 8−14
2538-4473
Vol.1/No.1
p. 15−29
2538-4473
Vol.1/No.1
G (exon 2), c.1366C>G (exon 3), c.3419 T>C (exon 16), c.3903 + 6C>T (intron 18) and c.4021+50G>C (intron 19). Conclusion: These common polymorphisms can be used by linkage analysis for the prenatal diagnosis and carrier detection in affected families with Wilson disease.]]>
p. 30−34
2538-4473
Vol.1/No.1
p. 35−41
2538-4473
Vol.1/No.1
p. 42−50
2538-4473
Vol.1/No.1
p. 51−60
2538-4473
Vol.1/No.1
p. 61−67
2538-4473
Vol.1/No.1