330 related articles for article (PubMed ID: 23559863)
1. Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.
Liu F; Li P; Liu Y; Li W; Wong F; Du R; Wang L; Li C; Jiang F; Tang Z; Liu M
Mol Vis; 2013; 19():695-701. PubMed ID: 23559863
[TBL] [Abstract][Full Text] [Related]
2. A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family.
He X; Peng Q; Li S; Zhu P; Wu C; Rao C; Lin J; Lu X
Int J Pediatr Otorhinolaryngol; 2017 Aug; 99():40-43. PubMed ID: 28688563
[TBL] [Abstract][Full Text] [Related]
3. Novel USH2A compound heterozygous mutations cause RP/USH2 in a Chinese family.
Liu X; Tang Z; Li C; Yang K; Gan G; Zhang Z; Liu J; Jiang F; Wang Q; Liu M
Mol Vis; 2010 Mar; 16():454-61. PubMed ID: 20309401
[TBL] [Abstract][Full Text] [Related]
4. New splice site mutations in MYO7A causing Usher syndrome type 1: a study on a Chinese consanguineous family.
Lin Q; Yang D; Shen Z; Zhou X
Int Ophthalmol; 2023 Jun; 43(6):2091-2099. PubMed ID: 36484953
[TBL] [Abstract][Full Text] [Related]
5. Novel compound heterozygous mutations in MYO7A Associated with Usher syndrome 1 in a Chinese family.
Gao X; Wang GJ; Yuan YY; Xin F; Han MY; Lu JQ; Zhao H; Yu F; Xu JC; Zhang MG; Dong J; Lin X; Dai P
PLoS One; 2014; 9(7):e103415. PubMed ID: 25080338
[TBL] [Abstract][Full Text] [Related]
6. Compound heterozygous MYO7A mutations segregating Usher syndrome type 2 in a Han family.
Zong L; Chen K; Wu X; Liu M; Jiang H
Int J Pediatr Otorhinolaryngol; 2016 Nov; 90():150-155. PubMed ID: 27729122
[TBL] [Abstract][Full Text] [Related]
7. Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family.
Ma Y; Xiao Y; Zhang F; Han Y; Li J; Xu L; Bai X; Wang H
Int J Pediatr Otorhinolaryngol; 2016 Apr; 83():179-85. PubMed ID: 26968074
[TBL] [Abstract][Full Text] [Related]
8. Seven novel mutations in the long isoform of the USH2A gene in Chinese families with nonsyndromic retinitis pigmentosa and Usher syndrome Type II.
Xu W; Dai H; Lu T; Zhang X; Dong B; Li Y
Mol Vis; 2011; 17():1537-52. PubMed ID: 21686329
[TBL] [Abstract][Full Text] [Related]
9. A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorder.
Xia H; Hu P; Yuan L; Xiong W; Xu H; Yi J; Yang Z; Deng X; Guo Y; Deng H
Mol Med Rep; 2017 Oct; 16(4):4241-4246. PubMed ID: 28731162
[TBL] [Abstract][Full Text] [Related]
10. Novel mutations of MYO7A and USH1G in Israeli Arab families with Usher syndrome type 1.
Rizel L; Safieh C; Shalev SA; Mezer E; Jabaly-Habib H; Ben-Neriah Z; Chervinsky E; Briscoe D; Ben-Yosef T
Mol Vis; 2011; 17():3548-55. PubMed ID: 22219650
[TBL] [Abstract][Full Text] [Related]
11. Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness.
Ben Rebeh I; Morinière M; Ayadi L; Benzina Z; Charfedine I; Feki J; Ayadi H; Ghorbel A; Baklouti F; Masmoudi S
Mol Vis; 2010 Sep; 16():1898-906. PubMed ID: 21031134
[TBL] [Abstract][Full Text] [Related]
12. Identification of five novel mutations in the long isoform of the USH2A gene in Chinese families with Usher syndrome type II.
Dai H; Zhang X; Zhao X; Deng T; Dong B; Wang J; Li Y
Mol Vis; 2008; 14():2067-75. PubMed ID: 19023448
[TBL] [Abstract][Full Text] [Related]
13. Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
Riazuddin S; Nazli S; Ahmed ZM; Yang Y; Zulfiqar F; Shaikh RS; Zafar AU; Khan SN; Sabar F; Javid FT; Wilcox ER; Tsilou E; Boger ET; Sellers JR; Belyantseva IA; Riazuddin S; Friedman TB
Hum Mutat; 2008 Apr; 29(4):502-11. PubMed ID: 18181211
[TBL] [Abstract][Full Text] [Related]
14. Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2.
Rong W; Chen X; Zhao K; Liu Y; Liu X; Ha S; Liu W; Kang X; Sheng X; Zhao C
PLoS One; 2014; 9(5):e97808. PubMed ID: 24831256
[TBL] [Abstract][Full Text] [Related]
15. Detecting novel genetic mutations in Chinese Usher syndrome families using next-generation sequencing technology.
Qu LH; Jin X; Xu HW; Li SY; Yin ZQ
Mol Genet Genomics; 2015 Feb; 290(1):353-63. PubMed ID: 25252889
[TBL] [Abstract][Full Text] [Related]
16. Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1.
Nakanishi H; Ohtsubo M; Iwasaki S; Hotta Y; Takizawa Y; Hosono K; Mizuta K; Mineta H; Minoshima S
J Hum Genet; 2010 Dec; 55(12):796-800. PubMed ID: 20844544
[TBL] [Abstract][Full Text] [Related]
17. Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A.
Kumar A; Babu M; Kimberling WJ; Venkatesh CP
Mol Vis; 2004 Nov; 10():910-6. PubMed ID: 15592175
[TBL] [Abstract][Full Text] [Related]
18. Novel mutations in the USH1C gene in Usher syndrome patients.
Aparisi MJ; García-García G; Jaijo T; Rodrigo R; Graziano C; Seri M; Simsek T; Simsek E; Bernal S; Baiget M; Pérez-Garrigues H; Aller E; Millán JM
Mol Vis; 2010 Dec; 16():2948-54. PubMed ID: 21203349
[TBL] [Abstract][Full Text] [Related]
19. Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis.
Ben-Rebeh I; Grati M; Bonnet C; Bouassida W; Hadjamor I; Ayadi H; Ghorbel A; Petit C; Masmoudi S
Mol Vis; 2016; 22():827-35. PubMed ID: 27440999
[TBL] [Abstract][Full Text] [Related]
20. Next-generation sequencing identifies a novel compound heterozygous mutation in MYO7A in a Chinese patient with Usher Syndrome 1B.
Wei X; Sun Y; Xie J; Shi Q; Qu N; Yang G; Cai J; Yang Y; Liang Y; Wang W; Yi X
Clin Chim Acta; 2012 Nov; 413(23-24):1866-71. PubMed ID: 22898263
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
