Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study

BACKGROUND: tinnitus is a heterogeneous condition associated with audiological and/or mental disorders. Chronic, severe tinnitus is reported in 1% of the population and it shows a relevant heritability, according to twins, adoptees and familial aggregation studies. The genetic contribution to severe...

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Detalles Bibliográficos
Autores principales: Amanat, Sana, Gallego-Martinez, Alvaro, Sollini, Joseph, Perez-Carpena, Patricia, Espinosa-Sanchez, Juan M., Aran, Ismael, Soto-Varela, Andres, Batuecas‐Caletrio, Angel, Canlon, Barbara, May, Patrick, Cederroth, Christopher R., Lopez-Escamez, Jose A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047463/
https://www.ncbi.nlm.nih.gov/pubmed/33813136
http://dx.doi.org/10.1016/j.ebiom.2021.103309

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