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Identification of a distinct mutation spectrum in theSMPD1gene of Chinese patients with acid sphingomyelinase-deficient Niemann-Pick disease

✍ Scribed by Zhang, Huiwen; Wang, Yu; Gong, Zhuwen; Li, Xiaoyan; Qiu, Wenjuan; Han, Lianshu; Ye, Jun; Gu, Xuefan

No coin nor oath required. For personal study only.

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