Novel OTOF pathogenic variant segregating with non-syndromic hearing loss in a consanguineous family from tribal Rajouri in Jammu and Kashmir
Author:
Funder
UGC Start Up grant, New Delhi, India
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
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1. Association of recurrent A1090E variant of OTOFERLIN (OTOF) gene with non-syndromic hereditary sensorineural hearing loss in Pakistani population;Khyber Medical University Journal;2023-12-31
2. A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options;Clinical Genetics;2022-09-29
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4. Genetics Landscape of Nonsyndromic Hearing Loss in Indian Populations;Journal of Pediatric Genetics;2021-12-14
5. Protection of Cochlear Ribbon Synapses and Prevention of Hidden Hearing Loss;Neural Plasticity;2020-11-01
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