患有阅读障碍的儿童的整体外组测序涉及CLDN3和离子通道基因的罕见变异

Krzysztof Marianski1, Joel B Talcott2, John Stein3

  • 1School of Medicine, University of St Andrews, St Andrews, UK.

Human genetics
|December 24, 2025
PubMed
概括

罕见的遗传变异导致发育性阅读障碍,这是影响儿童的阅读困难. 这项研究确定了包括CLDN3在内的五个关键基因,在阅读障碍病例中具有高影响变异,这表明罕见变异起着重要作用.

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