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Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss

✍ Scribed by Jianzhong Li; Jing Cheng; Yanping Lu; Yu Lu; Aiting Chen; Yi Sun; Dongyang Kang; Xin Zhang; Pu Dai; Dongyi Han; Huijun Yuan

No coin nor oath required. For personal study only.

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