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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...
Autores principales: | Hytönen, Marjo K., Niskanen, Julia E., Arumilli, Meharji, Brookhart-Knox, Casey A., Donner, Jonas, Lohi, Hannes |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
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 |
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