Usher Syndrome: Genetics and Molecular Links of Hearing Loss and Directions for Therapy

Usher syndrome (USH) is an autosomal recessive (AR) disorder that permanently and severely affects the senses of hearing, vision, and balance. Three clinically distinct types of USH have been identified, decreasing in severity from Type 1 to 3, with symptoms of sensorineural hearing loss (SNHL), ret...

Descripción completa

Detalles Bibliográficos
Autores principales: Whatley, Meg, Francis, Abbie, Ng, Zi Ying, Khoh, Xin Ee, Atlas, Marcus D., Dilley, Rodney J., Wong, Elaine Y. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642844/
https://www.ncbi.nlm.nih.gov/pubmed/33193648
http://dx.doi.org/10.3389/fgene.2020.565216

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642844/
https://www.ncbi.nlm.nih.gov/pubmed/33193648
http://dx.doi.org/10.3389/fgene.2020.565216

Ejemplares similares