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Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.
BMC Med Genet. 2020 Nov 18;21(1):226. doi: 10.1186/s12881-020-01168-x.
BMC Med Genet. 2020.
PMID: 33208113
Free PMC article.
Whole exome sequencing identifies both nuclear and mitochondrial variations in an Iranian family with non-syndromic hearing loss.
Khatami S, Rokni-Zadeh H, Mohsen-Pour N, Biglari A, Changi-Ashtiani M, Shahrooei M, Shahani T.
Khatami S, et al.
Mitochondrion. 2019 May;46:321-325. doi: 10.1016/j.mito.2018.08.006. Epub 2018 Sep 8.
Mitochondrion. 2019.
PMID: 30205178
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