论文信息 - Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2. - 字舞流文

Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2.

J. Seidman | M. Bitner-Glindzicz | Xiangyin Kong | R. Eavey | A. Kantardzhieva | X. Liu | C. Seidman | D. Yan | B. Han | Heng Xu | M. Teng | P. Dai | X. Ouyang | Huijun Yuan | L. Du | Dongyi Han | Jianzhong Li | Jing Cheng | Xu Li | Zhanguo Jin | Youqin Wang | Zheng-Yi Chen