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2017•International Journal of Pediatric OtorhinolaryngologyRequires access

A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family

Xiaoguang He, Qi Peng, Siping Li, Pengyuan Zhu, Chunqiu Wu, Chunbao Rao, Jingqi Lin, Xiaomei Lu

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Key concepts: Proband, Retinitis pigmentosa, Genetics, Usher syndrome, Hearing loss, Compound heterozygosity, Sanger sequencing, Mutation

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A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family — Research Paper | ScholarLens