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一种新的错义致病变异TMEM53在伊朗家庭与颅管发育不良,Ikegawa型
论文通过对一个伊朗家族的研究,发现了 TMEM53 基因的新型纯合错义变异,为 CTDI 的诊断和治疗提供了新的见解。研究建议早期进行全面的临床和基因评估,并给予适当治疗,这将有助于改善 CTDI 患者的预后。这不仅为该家族患者带来了新的希望,也为未来更多 CTDI 病例的诊治提供了参考依据。
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