Whole-Exome Sequencing Identifies Three Novel TTN Variants in Chinese Families with Dilated Cardiomyopathy

被引：0
|
作者：
Dong, Yi [1 ,2 ]
Xiao, Jiao [3 ]
Cao, Gaohui [2 ]
Jin, Jieyuan [2 ]
Sheng, Yve [2 ]
Chen, Yaqin [1 ]
Guo, Yadong [3 ]
Xiang, Rong [2 ]
机构：
[1] Cent South Univ, Xiangya Hosp 2, Dept Cardiol, Changsha 410011, Peoples R China
[2] Cent South Univ, Sch Life Sci, Dept Cell Biol, Changsha 410013, Peoples R China
[3] Cent South Univ, Sch Basic Med Sci, Dept Forens Sci, Changsha, Peoples R China
来源：
CARDIOVASCULAR INNOVATIONS AND APPLICATIONS | 2024年 / 9卷 / 01期
关键词：
D O I：
10.15212/CVIA.2024.0040
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页数：3
相关论文
共 50 条
  • [31] Genetic characterization of dilated cardiomyopathy patients undergoing heart transplantation in the Chinese population by whole-exome sequencing
    Hong Lian
    Shen Song
    Wenzheng Chen
    Anteng Shi
    Haobin Jiang
    Shengshou Hu
    [J]. Journal of Translational Medicine, 21
  • [32] Genetic characterization of dilated cardiomyopathy patients undergoing heart transplantation in the Chinese population by whole-exome sequencing
    Lian, Hong
    Song, Shen
    Chen, Wenzheng
    Shi, Anteng
    Jiang, Haobin
    Hu, Shengshou
    [J]. JOURNAL OF TRANSLATIONAL MEDICINE, 2023, 21 (01)
  • [33] Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes
    Chen, Shitao
    Wang, Guishuan
    Zheng, Xiaoguo
    Ge, Shunna
    Dai, Yubing
    Ping, Ping
    Chen, Xiangfeng
    Liu, Guihua
    Zhang, Jing
    Yang, Yang
    Zhang, Xinzong
    Zhong, An
    Zhu, Yongtong
    Chu, Qingjun
    Huang, Yonghan
    Zhang, Yong
    Shen, Changli
    Yuan, Yiming
    Yuan, Qilong
    Pei, Xiuying
    Cheng, C. Yan
    Sun, Fei
    [J]. HUMAN MOLECULAR GENETICS, 2020, 29 (14) : 2451 - 2459
  • [34] Prevalence of TTR variants detected by whole-exome sequencing in hypertrophic cardiomyopathy
    Lopes, Luis R.
    Futema, Marta
    Akhtar, Mohammed M.
    Lorenzini, Massimiliano
    Pittman, Alan
    Syrris, Petros
    Elliott, Perry M.
    [J]. AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2019, 26 (04): : 243 - 247
  • [35] Whole-Exome Sequencing Revealed New Candidate Genes for Human Dilated Cardiomyopathy
    D'Agostino, Ylenia
    Palumbo, Domenico
    Rusciano, Maria Rosaria
    Strianese, Oriana
    Amabile, Sonia
    Di Rosa, Domenico
    De Angelis, Elena
    Visco, Valeria
    Russo, Fabio
    Alexandrova, Elena
    Salvati, Annamaria
    Giurato, Giorgio
    Nassa, Giovanni
    Tarallo, Roberta
    Galasso, Gennaro
    Ciccarelli, Michele
    Weisz, Alessandro
    Rizzo, Francesca
    [J]. DIAGNOSTICS, 2022, 12 (10)
  • [36] Whole-exome sequencing identifies rare pathogenic and candidate variants in sporadic Chinese Han deaf patients
    Zou, Songfeng
    Mei, Xueshuang
    Yang, Weiqiang
    Zhu, Rvfei
    Yang, Tao
    Hu, Hongyi
    [J]. CLINICAL GENETICS, 2020, 97 (02) : 352 - 356
  • [37] Family-Based Whole-Exome Sequencing for Identifying Novel Variants in Consanguineous Families with Schizophrenia
    Shirzad, Hadi
    Beiraghi, Narges
    Kachoui, Mojgan Ataei
    Akbari, Mohammad Taghi
    [J]. IRANIAN RED CRESCENT MEDICAL JOURNAL, 2017, 19 (02)
  • [38] Whole Exome Sequencing Identifies a Mutation in Transportin 3 as a Cause of Dilated Cardiomyopathy
    Li, Duanxiang
    Norton, Nadine
    Xu, Yan
    Wiley, David J.
    Luo, Chunyan
    Ouyang, Ping
    Siegfried, Jill D.
    Rampersaud, Evadnie
    Zchner, Stephan
    Mangos, Steve
    Durso, Gennaro Durso
    Martin, Eden
    Rieder, Mark J.
    Wang, Qing K.
    Nickerson, Deborah A.
    Hershberger, Ray E.
    [J]. CIRCULATION RESEARCH, 2011, 109 (12) : E56 - E57
  • [39] Whole-exome identifies germline variants in families with obstructive sleep apnea syndrome
    de Azevedo, Pedro Guimaraes
    Guimaraes, Maria de Lourdes Rabelo
    Albuquerque, Anna Luiza Braga
    Alves, Rayane Benfica
    Fernandes, Bianca Gomes
    de Melo, Flavia Marques
    Cardenas, Raony Guimaraes Correa Do Carmo Lisboa
    Friedman, Eitan
    De Marco, Luiz
    Bastos-Rodrigues, Luciana
    [J]. FRONTIERS IN GENETICS, 2023, 14
  • [40] Whole-exome sequencing identifies rare, functional CFHvariants in families with macular degeneration
    Yu, Yi
    Triebwasser, Michael P.
    Wong, Edwin K. S.
    Schramm, Elizabeth C.
    Thomas, Brett
    Reynolds, Robyn
    Mardis, Elaine R.
    Atkinson, John P.
    Daly, Mark
    Raychaudhuri, Soumya
    Kavanagh, David
    Seddon, Johanna M.
    [J]. HUMAN MOLECULAR GENETICS, 2014, 23 (19) : 5283 - 5293
12345