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Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population.
Am J Med Genet B Neuropsychiatr Genet. 2020 Apr;183(3):172-180. doi: 10.1002/ajmg.b.32774. Epub 2019 Dec 19.
Am J Med Genet B Neuropsychiatr Genet. 2020.
PMID: 31854501
Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss.
Ramzan K, Al-Numair NS, Al-Ageel S, Elbaik L, Sakati N, Al-Hazzaa SAF, Al-Owain M, Imtiaz F.
Ramzan K, et al. Among authors: al ageel s.
Genes (Basel). 2020 Dec 9;11(12):1474. doi: 10.3390/genes11121474.
Genes (Basel). 2020.
PMID: 33316915
Free PMC article.
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Utility of whole exome sequencing in the diagnosis of Usher syndrome: Report of novel compound heterozygous MYO7A mutations.
Ramzan K, Al-Owain M, Huma R, Al-Hazzaa SAF, Al-Ageel S, Imtiaz F, Al-Sayed M.
Ramzan K, et al. Among authors: al ageel s.
Int J Pediatr Otorhinolaryngol. 2018 May;108:17-21. doi: 10.1016/j.ijporl.2018.02.016. Epub 2018 Feb 14.
Int J Pediatr Otorhinolaryngol. 2018.
PMID: 29605349
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