Screening Consanguineous Families for Hearing Loss Using the MiamiOtoGenes Panel

Background: Hearing loss (HL) is one of the most common and genetically heterogeneous sensory disorders in humans. Genetic causes underlie 50–60% of all HL and the majority of these cases exhibit an autosomal recessive model of inheritance. Methods: In our study, we used our targeted custom MiamiOto...

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Detalhes bibliográficos
Publicado no:Genet Test Mol Biomarkers
Main Authors: Kannan-Sundhari, Abhiraami, Yan, Denise, Saeidi, Kolsoum, Sahebalzamani, Afsaneh, Blanton, Susan H., Liu, Xue Zhong
Formato: Artigo
Idioma:Inglês
Publicado em: Mary Ann Liebert, Inc., publishers 2020
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7585618/
https://ncbi.nlm.nih.gov/pubmed/32991204
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2020.0153
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