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23 天
探秘 KBG 综合征:从三位患者身上解锁罕见病的诊疗新密码
为解决 KBG 综合征临床和基因组特征不明确等问题,意大利研究人员开展对相关患者的研究。结果发现患者临床和基因特征多样,明确了诊断方法。推荐阅读,助您深入了解罕见病研究,为相关领域提供新思路。 KBG 综合征(MIM #148050)是一种极为罕见的遗传疾病 ...
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