Article

MPZL2—A common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population

2023-08-31

Abstract excerpt

<h4>Background: </h4> Mutations in MPZL2 , the characteristic genetic etiology of autosomal recessive deafness loci 111 (DFNB111), cause non-syndromic and moderate sensorineural hearing loss. <h4>Methods: </h4>: In this study, we analyzed the phenotype and genotype of 8 pedigrees consisting of 10 deaf patients with bi-allelic pathogenic or likely pathogenic variants in MPZL2 . These patients were identified from...

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Literature Corpus work: 3c0da273-f396-5d67-81de-26ae929dc167
DOI: 10.21203/rs.3.rs-3177325/v1

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