Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson disease
Abstract Background Wilson disease (OMIM # 277900) is a autosomal recessive disorder characterized by accumulation of copper in liver and brain. The accumulation of copper resulting in oxidative stress and eventually cell death. The disease has an onset in a childhood and result in a significant neu...
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| Main Authors: | , , , , , , , , , |
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| Format: | Book |
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BMC,
2018-06-01T00:00:00Z.
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