Literature DB >> 31445392

Identification of a novel CDH23 gene variant associated with non-syndromic progressive hearing loss in a Chinese family: Individualized hearing rehabilitation guided by genetic diagnosis.

Ying Chen1, Yun Li2, Yan Ren3, Haifeng Li4, Meiping Huang5, Huan Jia6, Tao Yang7, Zhaoyan Wang8, Zhiwu Huang9, Hao Wu10.   

Abstract

Entities:  

Keywords:  CDH23; Genetic diagnosis; Hearing rehabilitation; Non-syndromic hearing loss; Progressive hearing loss

Year:  2019        PMID： 31445392     DOI： 10.1016/j.ijporl.2019.109649

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN： 0165-5876            Impact factor:   1.675


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  1 in total

1.  Genomic Regions 10q22.2, 17q21.31, and 2p23.1 Can Contribute to a Lower Lung Function in African Descent Populations.

Authors:  Héllen Fonseca; Thiago M da Silva; Mariana Saraiva; Meddly L Santolalla; Hanaisa P Sant'Anna; Nathalia M Araujo; Natália P Lima; Raimon Rios; Eduardo Tarazona-Santos; Bernardo L Horta; Alvaro Cruz; Mauricio L Barreto; Camila A Figueiredo
Journal:  Genes (Basel)       Date:  2020-09-04       Impact factor: 4.096
  1 in total

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