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    Identification of a novel compound heterozygous mutation in PTPRQ in a DFNB84 family with prelingual sensorineural hearing impairment

    With a prevalence of 0.1 %, hearing loss is among the most common sensory impairments and affects several million people around the world. Identification of deafness-related genes or loci may facilitate basic...

    Qing Sang, Honglin Mei, Ahan Kuermanhan, Ruizhi Feng… in Molecular Genetics and Genomics (2015)