222 related articles for article (PubMed ID: 36401330)
21. [Analysis of MYO15A variation in children with DFNB3].
Ren SM; Wu QH; Jiao ZH; Chen YB; Chen C; Kong XD; Qin ZB
Zhonghua Er Ke Za Zhi; 2020 Oct; 58(10):818-823. PubMed ID: 32987461
[No Abstract] [Full Text] [Related]
22. A novel nonsense mutation in MYO15A is associated with non-syndromic hearing loss: a case report.
Ma D; Shen S; Gao H; Guo H; Lin Y; Hu Y; Zhang R; Wang S
BMC Med Genet; 2018 Aug; 19(1):133. PubMed ID: 30068307
[TBL] [Abstract][Full Text] [Related]
23. Recurrent and private MYO15A mutations are associated with deafness in the Turkish population.
Cengiz FB; Duman D; Sirmaci A; Tokgöz-Yilmaz S; Erbek S; Oztürkmen-Akay H; Incesulu A; Edwards YJ; Ozdag H; Liu XZ; Tekin M
Genet Test Mol Biomarkers; 2010 Aug; 14(4):543-50. PubMed ID: 20642360
[TBL] [Abstract][Full Text] [Related]
24. Compound Heterozygous Mutations in
Xu P; Xu J; Peng H; Yang T
Neural Plast; 2020; 2020():8872185. PubMed ID: 32802042
[TBL] [Abstract][Full Text] [Related]
25. A novel recessive truncating mutation in MYO15A causing prelingual sensorineural hearing loss.
Li W; Guo L; Li Y; Wu Q; Li Q; Li H; Dai C
Int J Pediatr Otorhinolaryngol; 2016 Feb; 81():92-5. PubMed ID: 26810297
[TBL] [Abstract][Full Text] [Related]
26. Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees.
Nasrniya S; Miar P; Narrei S; Sepehrnejad M; Nilforoush MH; Abtahi H; Tabatabaiefar MA
Lab Med; 2022 Mar; 53(2):111-122. PubMed ID: 34388253
[TBL] [Abstract][Full Text] [Related]
27. Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in
Wang L; Zhao L; Peng H; Xu J; Lin Y; Yang T; Wu H
Neural Plast; 2020; 2020():6350479. PubMed ID: 32617096
[TBL] [Abstract][Full Text] [Related]
28. Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locus.
Belguith H; Aifa-Hmani M; Dhouib H; Said MB; Mosrati MA; Lahmar I; Moalla J; Charfeddine I; Driss N; Arab SB; Ghorbel A; Ayadi H; Masmoudi S
Genet Test Mol Biomarkers; 2009 Feb; 13(1):147-51. PubMed ID: 19309289
[TBL] [Abstract][Full Text] [Related]
29. Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.
Liburd N; Ghosh M; Riazuddin S; Naz S; Khan S; Ahmed Z; Riazuddin S; Liang Y; Menon PS; Smith T; Smith AC; Chen KS; Lupski JR; Wilcox ER; Potocki L; Friedman TB
Hum Genet; 2001 Nov; 109(5):535-41. PubMed ID: 11735029
[TBL] [Abstract][Full Text] [Related]
30. Identification of Novel Compound Heterozygous
Wang XH; Xie L; Chen S; Xu K; Bai X; Jin Y; Qiu Y; Liu XZ; Sun Y; Kong WJ
Neural Plast; 2021; 2021():9957712. PubMed ID: 34093702
[TBL] [Abstract][Full Text] [Related]
31. Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.
Nal N; Ahmed ZM; Erkal E; Alper OM; Lüleci G; Dinç O; Waryah AM; Ain Q; Tasneem S; Husnain T; Chattaraj P; Riazuddin S; Boger E; Ghosh M; Kabra M; Riazuddin S; Morell RJ; Friedman TB
Hum Mutat; 2007 Oct; 28(10):1014-9. PubMed ID: 17546645
[TBL] [Abstract][Full Text] [Related]
32. Hearing Features and Cochlear Implantation Outcomes in Patients With Pathogenic MYO15A Variants: a Multicenter Observational Study.
Chen PY; Tsai CY; Wu JL; Li YL; Wu CM; Chen KC; Hwang CF; Wu HP; Lin HC; Cheng YF; Lo MY; Liu TC; Yang TH; Chen PL; Hsu CJ; Wu CC
Ear Hear; 2022 Jul-Aug 01; 43(4):1198-1207. PubMed ID: 34974475
[TBL] [Abstract][Full Text] [Related]
33. Prioritized sequencing of the second exon of MYO15A reveals a new mutation segregating in a Pakistani family with moderate to severe hearing loss.
Bashir R; Fatima A; Naz S
Eur J Med Genet; 2012 Feb; 55(2):99-102. PubMed ID: 22245518
[TBL] [Abstract][Full Text] [Related]
34. Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.
Khatami S; Askari M; Bahreini F; Hashemzadeh-Chaleshtori M; Hematian S; Asgharzade S
BMC Med Genet; 2020 Nov; 21(1):226. PubMed ID: 33208113
[TBL] [Abstract][Full Text] [Related]
35. Three
Zhang F; Xu L; Xiao Y; Li J; Bai X; Wang H
Neural Plast; 2018; 2018():5898025. PubMed ID: 29849560
[TBL] [Abstract][Full Text] [Related]
36. Identification of a novel homozygous mutation in the MYO15A gene in a Kazakh family with non-syndromic hearing loss.
Zhou H; Kuermanhan A; Zhang Z; Wang W; Dong J; Zhou Z; Mu J; Zhao L; Wang J; Li B; Chen B
Int J Pediatr Otorhinolaryngol; 2019 Oct; 125():128-132. PubMed ID: 31301639
[TBL] [Abstract][Full Text] [Related]
37. Identification of Novel and Recurrent Variants in
Booth KT; Hirsch Y; Vardaro AC; Ekstein J; Yefet D; Quint A; Weiden T; Corey DP
Front Genet; 2021; 12():737782. PubMed ID: 34733312
[TBL] [Abstract][Full Text] [Related]
38. Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss.
Mehregan H; Mohseni M; Jalalvand K; Arzhangi S; Nikzat N; Banihashemi S; Kahrizi K; Najmabadi H
Int J Pediatr Otorhinolaryngol; 2019 Feb; 117():115-126. PubMed ID: 30579064
[TBL] [Abstract][Full Text] [Related]
39. Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing.
Zarepour N; Koohiyan M; Taghipour-Sheshdeh A; Nemati-Zargaran F; Saki N; Mohammadi-Asl J; Tabatabaiefar MA; Hashemzadeh-Chaleshtori M
Audiol Neurootol; 2019; 24(1):25-31. PubMed ID: 30943474
[TBL] [Abstract][Full Text] [Related]
40. 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; 14():72. PubMed ID: 23865914
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
