在有 aminotransferases 的举起的一个 9 月的老男孩的遗传上证实的威尔森疾病

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Wilson disease (WD) is an autosomal recessive disorder of copper transport caused by alteration of the adenosine triphosphatase 7B gene. It is rare to diagnose WD below the age of three years. Molecular genetic testing is one of the most important diagnos
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