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    MYRF gene mutation leading to coronary artery anomaly combined with 46,XY sex development disorder, a case report and literature review

    MYRF gene mutation leading to coronary artery anomaly combined with 46,XY sex development disorder, a case report and literature review by Jianhua Ding, Zhenyu Lv, Zhen Zhen, Yong Gai, Yanyan Xiao

    Published 2025-08-01
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