Progressive Dominant Hearing Loss (Autosomal Dominant Deafness-41) and P2RX2 Gene Mutations: A Phenotype-Genotype Study.

Liu, Xue Zhong; Yan, Denise; Mittal, Rahul; Ballard, Megan E; Feng, Yong

Liu, Xue Zhong; Yan, Denise; Mittal, Rahul; Ballard, Megan E; Feng, Yong.

Afiliación

Liu XZ; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida, U.S.A.
Yan D; Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, U.S.A.
Mittal R; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida, U.S.A.
Ballard ME; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida, U.S.A.
Feng Y; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida, U.S.A.

Laryngoscope ; 130(7): 1657-1663, 2020 07.

Article en En | MEDLINE | ID: mdl-31593348

Asunto(s)

Pérdida Auditiva Sensorineural/genética; Receptores Purinérgicos P2X2/genética; Adulto; Progresión de la Enfermedad; Femenino; Estudios de Seguimiento; Genotipo; Humanos; Estudios Longitudinales; Masculino; Persona de Mediana Edad; Mutación; Linaje; Fenotipo; Factores Sexuales

Palabras clave

P2RX2; Genetics; autosomal dominant deafness-41; hearing loss

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores Purinérgicos P2X2 / Pérdida Auditiva Sensorineural Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Laryngoscope Asunto de la revista: OTORRINOLARINGOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

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