证实THOC6在智力残疾病因学中的候选地位。 - Suppr | 超能文献

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Confirming the candidacy of THOC6 in the etiology of intellectual disability.证实THOC6在智力残疾病因学中的候选地位。

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Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping.THOC6基因的常染色体隐性突变导致智力障碍：综合征的描述需要正向和反向表型分析。

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Clinical and functional characterization of recurrent missense variants implicated in THOC6-related intellectual disability.反复出现的错义变异与 THOC6 相关智力障碍的临床和功能特征。

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Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation.临床和神经认知特征分析一家族新型 MED12 基因移码突变。

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[Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects].NONO基因的突变导致综合征性智力残疾和抑制性突触缺陷

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Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration.AIMP1基因中的错义变异与无神经退行性变的常染色体隐性智力障碍有关。

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THOC6 is a novel biomarker of glioma and a target of anti-glioma drugs: An analysis based on bioinformatics and molecular docking.THOC6 是一种新型的脑胶质瘤标志物和抗脑胶质瘤药物靶点：基于生物信息学和分子对接的分析。

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TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome.TREX 四聚体结构破坏改变了 THOC6 智力障碍综合征中皮质发生所必需的 RNA 加工。

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Structure of the human core transcription-export complex reveals a hub for multivalent interactions.