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Intronic OTOF mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorder.
Mohammadi, Sanaz; Khamirani, Hossein Jafari; Zoghi, Sina; Dastgheib, Seyed Alireza; Bagher Tabei, Seyed Mohammad; Talebzadeh, Mahdieh; Adibi, Mohammad Hossein; Dianatpour, Mehdi.
Affiliation
  • Mohammadi S; Comprehensive Medical Genetic Center, Shiraz University of Medical Sciences, Shiraz 71936-13311, Iran.
J Genet ; 1022023.
Article in En | MEDLINE | ID: mdl-36988134
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Collection: 01-internacional Database: MEDLINE Main subject: Hearing Loss, Central / Membrane Proteins Type of study: Etiology_studies / Prognostic_studies Limits: Humans Language: En Journal: J Genet Year: 2023 Document type: Article Affiliation country: Iran Country of publication: India
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Hearing Loss, Central / Membrane Proteins Type of study: Etiology_studies / Prognostic_studies Limits: Humans Language: En Journal: J Genet Year: 2023 Document type: Article Affiliation country: Iran Country of publication: India