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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

275 related items for PubMed ID: 26308726

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  • 7. Report of a Novel Splicing Mutation in the MYO15A Gene in a Patient With Sensorineural Hearing Loss and Spectrum of the MYO15A Mutations.
    Akbariazar E, Vahabi A, Abdi Rad I.
    Clin Med Insights Case Rep; 2019; 12():1179547619871907. PubMed ID: 31579092
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  • 8. MYO15A splicing mutations in hearing loss: A review literature and report of a novel mutation.
    Motavaf M, Soveizi M, Maleki M, Mahdieh N.
    Int J Pediatr Otorhinolaryngol; 2017 May; 96():35-38. PubMed ID: 28390610
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  • 9. Identification of novel variants in MYO15A, OTOF, and RDX with hearing loss by next-generation sequencing.
    Bai X, Nian S, Feng L, Ruan Q, Luo X, Wu M, Yan Z.
    Mol Genet Genomic Med; 2019 Aug; 7(8):e808. PubMed ID: 31250571
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  • 11. Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss.
    Zheng K, Lin S, Gao J, Chen S, Su J, Liu Z, Duan S.
    BMC Med Genomics; 2024 Jan 02; 17(1):4. PubMed ID: 38167320
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  • 14. Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss.
    Diaz-Horta O, Duman D, Foster J, Sırmacı A, Gonzalez M, Mahdieh N, Fotouhi N, Bonyadi M, Cengiz FB, Menendez I, Ulloa RH, Edwards YJ, Züchner S, Blanton S, Tekin M.
    PLoS One; 2012 Jan 02; 7(11):e50628. PubMed ID: 23226338
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  • 16. Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss.
    Zardadi S, Razmara E, Asgaritarghi G, Jafarinia E, Bitarafan F, Rayat S, Almadani N, Morovvati S, Garshasbi M.
    Mol Genet Genomic Med; 2020 Dec 02; 8(12):e1550. PubMed ID: 33205915
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  • 17. Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families.
    Woo HM, Park HJ, Baek JI, Park MH, Kim UK, Sagong B, Koo SK.
    BMC Med Genet; 2013 Jul 17; 14():72. PubMed ID: 23865914
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  • 18. Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A.
    Yang JY, Wang WQ, Han MY, Huang SS, Wang GJ, Su Y, Xu JC, Fu Y, Kang DY, Yang K, Zhang X, Liu X, Gao X, Yuan YY, Dai P.
    BMC Med Genomics; 2022 Nov 18; 15(1):241. PubMed ID: 36401330
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