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首页> 外文期刊>Amyloid: the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis >AApoAIL75P amyloidosis causes cirrhosis-like appearance of the liver in the absence of laboratory or clinical signs of hepatic dysfunction
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AApoAIL75P amyloidosis causes cirrhosis-like appearance of the liver in the absence of laboratory or clinical signs of hepatic dysfunction

机译:AApoAIL75P淀粉样变性在缺乏肝功能异常的实验室或临床体征的情况下会引起肝硬化样外观

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摘要

Hereditary systemic amyloidosis is a genetically and clinically heterogeneous group of diseases caused by deposits of insoluble proteins within tissues. The majority of cases are due to a mutation of the transthyretin gene (TTR); however, variants of other proteins such as apolipoproteinAI (ApoAI) [1] have been found to be associated with hereditary amyloidosis. AApoAI amyloidosis has been first described by van Allen et al.
机译:遗传性系统性淀粉样变性病是由组织内不溶性蛋白质沉积引起的遗传和临床异质性疾病组。大多数情况是由于运甲状腺素蛋白基因(TTR)的突变引起的。然而,已发现其他蛋白质的变异体,例如载脂蛋白AI(ApoAI)[1]与遗传性淀粉样变性有关。 van Allen等人首先描述了AApoAI淀粉样变性。

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