【摘 要】
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Objective This study was to identify Proteolipid protein 1 (PLP1) mutations in 33 unrelated Chinese patients (P1-33) with Pelizaeus-Merzbacher disease (PMD)
【机 构】
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Department of Pediatrics, Peking University First Hospital, Beijing 100034, China
【出 处】
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中国神经科学学会第九届全国学术会议暨第五届会员代表大会