Missense variant in LOXHD1 is associated with canine nonsyndromic hearing loss

Hearing loss is a common sensory deficit in both humans and dogs. In canines, the genetic basis is largely unknown, as genetic variants have only been identified for a syndromic form of hearing impairment. We observed a congenital or early-onset sensorineural hearing loss in a Rottweiler litter. Ass...

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Detalles Bibliográficos
Autores principales: Hytönen, Marjo K., Niskanen, Julia E., Arumilli, Meharji, Brookhart-Knox, Casey A., Donner, Jonas, Lohi, Hannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8521602/
https://www.ncbi.nlm.nih.gov/pubmed/33983508
http://dx.doi.org/10.1007/s00439-021-02286-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8521602/
https://www.ncbi.nlm.nih.gov/pubmed/33983508
http://dx.doi.org/10.1007/s00439-021-02286-z

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