Exploring DIAPH1 gene mutations in patients with sensorineural hearing loss of unknown etiology in Northern Spain.

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Bibliographic Details
Title: Exploring DIAPH1 gene mutations in patients with sensorineural hearing loss of unknown etiology in Northern Spain.
Authors: González-Aguado R; Faculty of Medicine, University of Cantabria, Spain; Department of Otolaryngology, Hospital Universitario Marqués de Valdecilla, Santander, Cantabria, Spain; Institute for Research Marqués de Valdecilla (IDIVAL), 39011 Santander, Spain. Electronic address: rocio.gonzaleza@scsalud.es., Veiga-Alonso A; Faculty of Medicine, University of Cantabria, Spain; Department of Otolaryngology, Hospital Universitario Marqués de Valdecilla, Santander, Cantabria, Spain. Electronic address: aida.veiga@scsalud.es., Onecha-De La Fuente E; Department of Genetics, Hospital Universitario Marqués de Valdecilla, Santander, Cantabria, Spain; Cellular Signaling and Therapeutic Targets In Cancer Laboratory, Institute for Research Marqués de Valdecilla (IDIVAL), 39011 Santander, Spain. Electronic address: mariaesther.onecha@scsalud.es., Morales-Angulo C; Faculty of Medicine, University of Cantabria, Spain; Head of the Department of Otolaryngology, Hospital Universitario Marqués de Valdecilla, Santander, Cantabria, Spain; Cell Cycle, Stem Cell Fate and Cancer Laboratory, Institute for Research Marqués de Valdecilla (IDIVAL), 39011 Santander, Spain.
Source: Acta otorrinolaringologica espanola [Acta Otorrinolaringol Esp (Engl Ed)] 2025 Sep-Oct; Vol. 76 (5), pp. 512269. Date of Electronic Publication: 2025 Jul 10.
Publication Type: Journal Article; Observational Study
Journal Info: Publisher: Elsevier España Country of Publication: Spain NLM ID: 101770938 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2173-5735 (Electronic) Linking ISSN: 21735735 NLM ISO Abbreviation: Acta Otorrinolaringol Esp (Engl Ed) Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2173-5735
DOI:10.1016/j.otoeng.2025.512269