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3. Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss. Atik T; Onay H; Aykut A; Bademci G; Kirazli T; Tekin M; Ozkinay F PLoS One; 2015; 10(11):e0142154. PubMed ID: 26561413 [TBL] [Abstract][Full Text] [Related]
4. Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey. Duman D; Sirmaci A; Cengiz FB; Ozdag H; Tekin M Genet Test Mol Biomarkers; 2011; 15(1-2):29-33. PubMed ID: 21117948 [TBL] [Abstract][Full Text] [Related]
5. Identification of homozygous mutations for hearing loss. Dianatpour M; Smith E; Hashemi SB; Farazifard MA; Nezafat N; Razban V; Mani A Gene; 2021 Apr; 778():145464. PubMed ID: 33524517 [TBL] [Abstract][Full Text] [Related]
6. Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing. Yang T; Wei X; Chai Y; Li L; Wu H Orphanet J Rare Dis; 2013 Jun; 8():85. PubMed ID: 23767834 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Whole exome sequencing of six Chinese families with hereditary non-syndromic hearing loss. Liang P; Chen F; Wang S; Li Q; Li W; Wang J; Chen J; Zha D Int J Pediatr Otorhinolaryngol; 2021 Sep; 148():110817. PubMed ID: 34265623 [TBL] [Abstract][Full Text] [Related]
9. Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness. Riahi Z; Bonnet C; Zainine R; Louha M; Bouyacoub Y; Laroussi N; Chargui M; Kefi R; Jonard L; Dorboz I; Hardelin JP; Salah SB; Levilliers J; Weil D; McElreavey K; Boespflug OT; Besbes G; Abdelhak S; Petit C PLoS One; 2014; 9(6):e99797. PubMed ID: 24926664 [TBL] [Abstract][Full Text] [Related]
10. Genetic causes of moderate to severe hearing loss point to modifiers. Naz S; Imtiaz A; Mujtaba G; Maqsood A; Bashir R; Bukhari I; Khan MR; Ramzan M; Fatima A; Rehman AU; Iqbal M; Chaudhry T; Lund M; Brewer CC; Morell RJ; Friedman TB Clin Genet; 2017 Apr; 91(4):589-598. PubMed ID: 27573290 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness. Trabelsi M; Bahri W; Habibi M; Zainine R; Maazoul F; Ghazi B; Chaabouni H; Mrad R Int J Pediatr Otorhinolaryngol; 2013 May; 77(5):714-6. PubMed ID: 23434199 [TBL] [Abstract][Full Text] [Related]
14. Autosomal recessive nonsyndromic deafness genes: a review. Duman D; Tekin M Front Biosci (Landmark Ed); 2012 Jun; 17(6):2213-36. PubMed ID: 22652773 [TBL] [Abstract][Full Text] [Related]
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16. Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss. Xiang YB; Xu CY; Xu YZ; Li HZ; Zhou LL; Xu XQ; Chen ZH; Tang SH Mol Genet Genomic Med; 2020 Dec; 8(12):e1539. PubMed ID: 33095980 [TBL] [Abstract][Full Text] [Related]
17. Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss. Budde BS; Aly MA; Mohamed MR; Breß A; Altmüller J; Motameny S; Kawalia A; Thiele H; Konrad K; Becker C; Toliat MR; Nürnberg G; Sayed EAF; Mohamed ES; Pfister M; Nürnberg P Clin Genet; 2020 Jul; 98(1):32-42. PubMed ID: 32279305 [TBL] [Abstract][Full Text] [Related]
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20. Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss. Sarmadi A; Nasrniya S; Narrei S; Nouri Z; Abtahi H; Tabatabaiefar MA Mol Biol Rep; 2020 Jul; 47(7):5355-5364. PubMed ID: 32623615 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]