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Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case report

BACKGROUND: Progressive bilateral sensorineural deafness in postlingual period may be linked to many different etiologies including genetic factors. Identification of the exact deafness cause may, therefore, be quite challenging. Here we present a family with late-onset hearing loss as an autosomal...

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Detalhes bibliográficos
Publicado no:BMC Med Genet
Main Authors: Varga, Lukas, Danis, Daniel, Skopkova, Martina, Masindova, Ivica, Slobodova, Zuzana, Demesova, Lucia, Profant, Milan, Gasperikova, Daniela
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6525401/
https://ncbi.nlm.nih.gov/pubmed/31101089
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-019-0806-y
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