Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations

Hereditary hearing impairment (HI) caused by recessive GJB2 mutations is a frequent sensory disorder. The results of the molecular-based studies of HI are widely used in various genetic test systems. However, the ethical aspects are less described than the genetic aspects. The concerns expressed by...

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Veröffentlicht in:J Community Genet
Hauptverfasser: Solovyev, Aisen V., Dzhemileva, Lilya U., Posukh, Olga L., Barashkov, Nikolay A., Bady-Khoo, Marita S., Lobov, Semen L., Popova, Natalya Yu., Romanov, Georgii P., Sazonov, Nikolay N., Bondar, Alexander A., Morozov, Igor V., Tomsky, Mikhail I., Fedorova, Sardana A., Khusnutdinova, Elza K.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Springer Berlin Heidelberg 2017
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Original Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5496838/
https://ncbi.nlm.nih.gov/pubmed/28324246
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12687-017-0299-3
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