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Novel Mutations in FKBP10 Cause Rare Autosomal Recessive Osteogenesis Imperfecta in Chinese Patients
【作 者】
：
【机 构】
：
Department of Endocrinology, Key Laboratory of Endocrinology of Ministry of Health, Peking Union Med
【出 处】
：
第八届国际骨质疏松及骨矿盐疾病学术会议
【发表日期】
：
2016年8期
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