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Editorial
. 2022 May 11;13(5):852.
doi: 10.3390/genes13050852.

Genetics of Hearing Impairment

Hannie Kremer  1   2   3 , Ignacio Del Castillo  4   5
Affiliations
Editorial

Genetics of Hearing Impairment

Hannie Kremer et al. Genes (Basel). .

Abstract

The inner ear is a complex structure at the cellular and molecular levels [...].

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Conflict of interest statement

The authors declare no conflict of interest.

References

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    1. Wonkam-Tingang E., Schrauwen I., Esoh K.K., Bharadwaj T., Nouel-Saied L.M., Acharya A., Nasir A., Adadey S.M., Mowla S., Leal S.M., et al. Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment. Genes. 2020;11:1249. doi: 10.3390/genes11111249. - DOI - PMC - PubMed
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    1. Domínguez-Ruiz M., Rodríguez-Ballesteros M., Gandía M., Gómez-Rosas E., Villamar M., Scimemi P., Mancini P., Rendtorff N.D., Moreno-Pelayo M.A., Tranebjaerg L., et al. Novel Pathogenic Variants in PJVK, the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory Neuropathy Spectrum Disorder. Genes. 2022;13:149. doi: 10.3390/genes13010149. - DOI - PMC - PubMed

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