KCNQ1 c.386+30787C>T

Variant ID: 11-2497501-C-T

NM_000218.2(KCNQ1):c.386+30787C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


The Role of Genetic Variants in the Susceptibility of Noise-Induced Hearing Loss.

Frontiers In Cellular Neuroscience
Chen, Xue-Min XM; Xue, Xin-Miao XM; Yu, Ning N; Guo, Wei-Wei WW; Yuan, Shuo-Long SL; Jiang, Qing-Qing QQ; Yang, Shi-Ming SM
Publication Date: 2022

Variant appearance in text: rs718579
PubMed Link: 35903368
Variant Present in the following documents:
  • Main text
  • fncel-16-946206.pdf
View BVdb publication page



Noise-Induced Hearing Loss: Updates on Molecular Targets and Potential Interventions.

Neural Plasticity
Mao, Huanyu H; Chen, Yan Y
Publication Date: 2021

Variant appearance in text: rs718579
PubMed Link: 34306060
Variant Present in the following documents:
  • Main text
  • NP2021-4784385.pdf
View BVdb publication page



Modeling susceptibility to drug-induced long QT with a panel of subject-specific induced pluripotent stem cells.

Elife
Stillitano, Francesca F; Hansen, Jens J; Kong, Chi-Wing CW; Karakikes, Ioannis I; Funck-Brentano, Christian C; Geng, Lin L; Scott, Stuart S; Reynier, Stephan S; Wu, Ma M; Valogne, Yannick Y; Desseaux, Carole C; Salem, Joe-Elie JE; Jeziorowska, Dorota D; Zahr, Noël N; Li, Ronald R; Iyengar, Ravi R; Hajjar, Roger J RJ; Hulot, Jean-Sébastien JS
Publication Date: 2017-01-30

Variant appearance in text: rs718579
PubMed Link: 28134617
Variant Present in the following documents:
  • Main text
  • elife-19406.pdf
View BVdb publication page