References in periodicals archive

(1996) to be the underlying cause of postlingual (DFNB8) hearing impairment.

Compound heterozygosity for a mild and severe mutation leads to postlingual hearing loss (DFNB8), whereas the combination of two severe mutations leads to profound hearing impairment with prelingual onset (DFNB10) [4].

Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan.

Non-syndromic Autosomal Recessive Deafness in Pakistani Population: Epidemiology and Genetics

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