DGCR8 microprocessor defect characterizes familial multinodular goiter with schwannomatosis

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DGCR8 microprocessor defect characterizes familial multinodular goiter with schwannomatosis

机译：DGCR8 微处理器缺陷表征家族性多结节性甲状腺肿伴神经鞘瘤病

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BACKGROUND. DICER1 is the only miRNA biogenesis component associated with an inherited tumor syndrome, featuring multinodular goiter (MNG) and rare pediatric-onset lesions. Other susceptibility genes for familial forms of MNG likely exist.

机译：背景。DICER1 是唯一与遗传性肿瘤综合征相关的 miRNA 生物发生成分，具有多结节性甲状腺肿（MNG）和罕见的儿科发病病变。可能存在家族性MNG的其他易感基因。

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《The Journal of Clinical Investigation: The Official Journal of the American Society for Clinical Investigation》 |2020年第3期|1479-1490|共12页
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正文语种英语
中图分类临床医学;
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DGCR8 microprocessor defect characterizes familial multinodular goiter with schwannomatosis

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