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Monozygotic twins discordant for single umbilical artery and congenital heart disease

✍ Scribed by Daisuke Nakayama; Hideaki Masuzaki; Shuichiro Yoshimura; Shingo Moriyama; Tadayuki Ishimaru

Book ID
113985585
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
105 KB
Volume
179
Category
Article
ISSN
1097-6868

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## Abstract Wilson's disease (WD) is an autosomal recessive disorder characterized by the functional disruption of the copper‐transporting protein adenosine triphosphatase 7B (ATP‐ase 7B). The disease is caused by mutations in __ATP7B__ gene. It seems that the type of mutation in __ATP7B__ only to