145 related articles for article (PubMed ID: 30173967)
1. Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss.
Moassass F; Al-Halabi B; Nweder MS; Al-Achkar W
Int J Pediatr Otorhinolaryngol; 2018 Oct; 113():110-114. PubMed ID: 30173967
[TBL] [Abstract][Full Text] [Related]
2. First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss.
Al-Achkar W; Al-Halabi B; Ali B; Moassass F
Int J Pediatr Otorhinolaryngol; 2017 Jan; 92():82-87. PubMed ID: 28012540
[TBL] [Abstract][Full Text] [Related]
3. Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment.
Montazer Zohour M; Tabatabaiefar MA; Dehkordi FA; Farrokhi E; Akbari MT; Chaleshtori MH
Genet Test Mol Biomarkers; 2012 Apr; 16(4):271-8. PubMed ID: 22077646
[TBL] [Abstract][Full Text] [Related]
4. [Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria].
Gallo-Terán J; Morales-Angulo C; del Castillo I; Villamar M; Moreno-Pelayo MA; García-Mantilla J; Moreno F
Acta Otorrinolaringol Esp; 2002 Oct; 53(8):563-71. PubMed ID: 12530196
[TBL] [Abstract][Full Text] [Related]
5. [Prevalence of common genetic mutations and clinical characteristics analysis in patients at different ages with nonsyndromic hearing impairment].
Zhang CQ; Chen BB; Chen YY; Liu XJ; Zheng J; Gao JJ; Huang SY; Nan BY; Zhang YY; Yu X; Guan MX
Yi Chuan; 2013 Mar; 35(3):352-8. PubMed ID: 23575541
[TBL] [Abstract][Full Text] [Related]
6. Prevalence of mitochondrial DNA mutations in sporadic patients with nonsyndromic sensorineural hearing loss.
Jiang H; Chen J; Li Y; Lin PF; He JG; Yang BB
Braz J Otorhinolaryngol; 2016; 82(4):391-6. PubMed ID: 26873147
[TBL] [Abstract][Full Text] [Related]
7. [Mitochondrial DNA A1555G mutation of seven families with nonsyndromic hearing loss].
Ou QS; Cheng ZJ; Yang B; Jiang L; Chen J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):550-4. PubMed ID: 19806580
[TBL] [Abstract][Full Text] [Related]
8. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
Lévêque M; Marlin S; Jonard L; Procaccio V; Reynier P; Amati-Bonneau P; Baulande S; Pierron D; Lacombe D; Duriez F; Francannet C; Mom T; Journel H; Catros H; Drouin-Garraud V; Obstoy MF; Dollfus H; Eliot MM; Faivre L; Duvillard C; Couderc R; Garabedian EN; Petit C; Feldmann D; Denoyelle F
Eur J Hum Genet; 2007 Nov; 15(11):1145-55. PubMed ID: 17637808
[TBL] [Abstract][Full Text] [Related]
9. Study of mitochondrial DNA A1555G and C1494T mutations in a large cohort of women individuals.
Wang L; Wang X; Cai X; Qiang R
Mitochondrial DNA A DNA Mapp Seq Anal; 2019 Mar; 30(2):222-225. PubMed ID: 29790807
[TBL] [Abstract][Full Text] [Related]
10. The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.
Kokotas H; Grigoriadou M; Korres GS; Ferekidou E; Papadopoulou E; Neou P; Giannoulia-Karantana A; Kandiloros D; Korres S; Petersen MB
Biochem Biophys Res Commun; 2009 Dec; 390(3):755-7. PubMed ID: 19835846
[TBL] [Abstract][Full Text] [Related]
11. The role of mitochondrial DNA mutations in hearing loss.
Ding Y; Leng J; Fan F; Xia B; Xu P
Biochem Genet; 2013 Aug; 51(7-8):588-602. PubMed ID: 23605717
[TBL] [Abstract][Full Text] [Related]
12. [Modifier factors influencing the phenotypic manifestation of the deafness associated mitochondrial DNA mutations].
YANG AF; ZHENG J; LV JX; GUAN MX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):165-71. PubMed ID: 21462128
[TBL] [Abstract][Full Text] [Related]
13. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides.
Estivill X; Govea N; Barceló E; Badenas C; Romero E; Moral L; Scozzri R; D'Urbano L; Zeviani M; Torroni A
Am J Hum Genet; 1998 Jan; 62(1):27-35. PubMed ID: 9490575
[TBL] [Abstract][Full Text] [Related]
14. Spectrum of genetic changes in patients with non-syndromic hearing impairment and extremely high carrier frequency of 35delG GJB2 mutation in Belarus.
Danilenko N; Merkulava E; Siniauskaya M; Olejnik O; Levaya-Smaliak A; Kushniarevich A; Shymkevich A; Davydenko O
PLoS One; 2012; 7(5):e36354. PubMed ID: 22567152
[TBL] [Abstract][Full Text] [Related]
15. Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutation.
Hutchin TP; Lench NJ; Arbuzova S; Markham AF; Mueller RF
Eur J Hum Genet; 2001 Jan; 9(1):56-8. PubMed ID: 11175301
[TBL] [Abstract][Full Text] [Related]
16. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.
Wu CC; Chiu YH; Chen PJ; Hsu CJ
Ear Hear; 2007 Jun; 28(3):332-42. PubMed ID: 17485982
[TBL] [Abstract][Full Text] [Related]
17. [Mitochondrial DNA mutations and aminoglycoside antibiotics and hearing loss].
Qu J; Wang J; Xu S
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1936-40. PubMed ID: 26911053
[TBL] [Abstract][Full Text] [Related]
18. Detection of deafness-causing mutations in the Greek mitochondrial genome.
Kokotas H; Grigoriadou M; Korres GS; Ferekidou E; Kandiloros D; Korres S; Petersen MB
Dis Markers; 2011; 30(6):283-9. PubMed ID: 21725156
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation.
Zhu Y; Li Q; Chen Z; Kun Y; Liu L; Liu X; Yuan H; Zhai S; Han D; Dai P
Mitochondrion; 2009 Nov; 9(6):418-28. PubMed ID: 19682603
[TBL] [Abstract][Full Text] [Related]
20. Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey.
Tekin M; Duman T; Boğoçlu G; İncesulu A; Çomak E; Fitoz S; Yılmaz E; İlhan I; Akar N
Eur J Pediatr; 2003 Mar; 162(3):154-158. PubMed ID: 12655418
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
