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MYO15A splicing mutations in hearing loss: A review literature and report of a novel mutation.
Motavaf M, Soveizi M, Maleki M, Mahdieh N. Motavaf M, et al. Int J Pediatr Otorhinolaryngol. 2017 May;96:35-38. doi: 10.1016/j.ijporl.2017.03.008. Epub 2017 Mar 6. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28390610 Review.
Non-syndromic SNHL accounts for nearly 70% of hereditary hearing loss and 80% of SNHL cases show an autosomal recessive mode of inheritance (ARNSHL). ...Analysis of this mutation within the family showed that the mutation segregates with hearing …
Non-syndromic SNHL accounts for nearly 70% of hereditary hearing loss and 80% of SNHL cases show an autosomal recess …
Genetic etiology of hearing loss in Iran.
Babanejad M, Beheshtian M, Jamshidi F, Mohseni M, Booth KT, Kahrizi K, Najmabadi H. Babanejad M, et al. Hum Genet. 2022 Apr;141(3-4):623-631. doi: 10.1007/s00439-021-02421-w. Epub 2022 Jan 20. Hum Genet. 2022. PMID: 35050400 Review.
Hearing loss (HL) is an etiologically heterogeneous disorder that affects around 5% of the world's population. ...Comprehensive studies using different strategies from linkage analysis to next-generation sequencing, especially exome-sequencing, have achieved signifi …
Hearing loss (HL) is an etiologically heterogeneous disorder that affects around 5% of the world's population. ...Comprehensiv …