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Su1749 Whole-Genome Sequencing of Monozygotic Twins Discordant for Crohn's Disease

✍ Scribed by Petersen, Britt S.; Spehlmann, Martina E.; Rosenstiel, Philip C.; Schreiber, Stefan; Franke, Andre

Book ID
122739487
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
166 KB
Volume
144
Category
Article
ISSN
0016-5085

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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