路透6月24日 - 美国食品和药物管理局周二表示，它正在调查两起杜氏肌营养不良症患者在接受Sarepta Therapeutics公司的SRPT.O基因疗法Elevidys后因急性肝功能衰竭而死亡的报告。
(为便利非英文母语者，路透将其报导自动化翻译为数种其他语言。由于自动化翻译可能有误，或未能包含所需语境，路透不保证自动化翻译文本的准确性，仅是为了便利读者而提供自动化翻译。对于因为使用自动化翻译功能而造成的任何损害或损失，路透不承担任何责任。)
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