A Prospective Study of Genetic Variants in Infants with Congenital Unilateral Sensorineural Hearing Loss.

Johansson, Marlin; Karltorp, Eva; Asp, Filip; Berninger, Erik

Johansson, Marlin; Karltorp, Eva; Asp, Filip; Berninger, Erik.

Afiliación

Johansson M; Division of Ear, Nose and Throat Diseases, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, 141 52 Stockholm, Sweden.
Karltorp E; Department of Audiology and Neurotology, Karolinska University Hospital, 141 86 Stockholm, Sweden.
Asp F; Division of Ear, Nose and Throat Diseases, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, 141 52 Stockholm, Sweden.
Berninger E; Department of Hearing Implants, Karolinska University Hospital, 141 86 Stockholm, Sweden.

J Clin Med ; 12(2)2023 Jan 07.

Article en En | MEDLINE | ID: mdl-36675424

Palabras clave

auditory dysfunction; congenital; etiology; genetic; genetic variants; pediatric; sensorineural hearing loss; unilateral hearing loss

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: J Clin Med Año: 2023 Tipo del documento: Article País de afiliación: Suecia

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google