Whole exome sequencing (WES) in a patient with a cardiac conduction defect and ventricular arrhythmias

被引:0
|
作者
Friedrich, C. [1 ]
Rinne, S. [2 ]
Zumhagen, S. [1 ]
Netter, M. [2 ]
Stallmeyer, B. [1 ]
Schulze-Bahr, E. [1 ]
Decher, N. [2 ]
机构
[1] Univ Hosp, Inst Genet Heart Dis, Dept Cardiovasc Med, Munster, Germany
[2] Univ Marburg, Inst Physiol & Pathophysiol, Marburg, Germany
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:420 / 421
页数:2
相关论文
共 50 条
  • [31] Next-generation Sequencing Panel for Autism and/or Intellectual Disability: A Comparable Alternative to Whole Exome Sequencing (WES)
    Bishay, D.
    Elloumi, Hzghal H.
    Stolar, D.
    Shanmugham, A.
    Zou, F.
    Scuffins, J.
    Brandt, T.
    ANNALS OF NEUROLOGY, 2017, 82 : S300 - S301
  • [32] Whole exome sequencing (WES) to define the genomic landscape of young lung cancer patients (pts).
    Wu, Xiaoliang
    Chen, Yanwen
    Zhu, Lin
    Stylianou, Eleni
    Barnholtz-Sloan, Jill
    Zhang, Zhenfeng
    Ma, Patrick C.
    JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)
  • [33] Cardiomyopathies (CMs): from clinical characterization to Whole Exome Sequencing (WES) analysis in Italian patients
    Alessandrini, Beatrice
    Lenarduzzi, Stefania
    Dal Ferro, Matteo
    Paldino, Alessia
    Sinagra, Gianfranco
    Gasparini, Paolo
    Girotto, Giorgia
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 138 - 138
  • [34] Clinical and genetic features of paroxysmal kinesigenic dyskinesia (PKD) studied with whole exome sequencing (WES)
    Xu, Z.
    Lu, Z.
    Lim, C. K.
    Low, S. C.
    Ng, E.
    Tan, A. H.
    Lim, S. Y.
    Tan, E. K.
    Tan, L.
    MOVEMENT DISORDERS, 2019, 34 : S227 - S228
  • [35] WHOLE EXOME SEQUENCING (WES) IDENTIFIES CILIOPATHY AND LATERALITY CANDIDATE GENES FOR BILIARY ATRESIA (BA)
    Berauer, John-Paul
    Mezina, Anya
    Sabo, Aniko
    Hegde, Madhuri
    Perlmutter, David H.
    Karpen, Saul J.
    GASTROENTEROLOGY, 2017, 152 (05) : S1064 - S1064
  • [36] Whole exome sequencing (WES) of methotrexate response/adverse event profile in rheumatoid arthritis patients
    Salam, Lobna Abdel
    Aldarwesh, Amal Q.
    Eleishi, Hatem H.
    EGYPTIAN RHEUMATOLOGIST, 2021, 43 (04): : 287 - 291
  • [37] Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous community
    Simon, Amos J.
    Golan, Adi Cohen
    Lev, Atar
    Stauber, Tali
    Barel, Ortal
    Somekh, Ido
    Klein, Christoph
    AbuZaitun, Omar
    Eyal, Eran
    Kol, Nitzan
    Unal, Ekrem
    Amariglio, Ninette
    Rechavi, Gideon
    Somech, Raz
    CLINICAL IMMUNOLOGY, 2020, 214
  • [38] MSI-WES: a simple approach for microsatellite instability testing using whole exome sequencing
    Ebili, Henry O.
    Agboola, Adedeji O. J.
    Rakha, Emad
    FUTURE ONCOLOGY, 2021, 17 (27) : 3595 - 3606
  • [39] WHOLE-EXOME-SEQUENCING (WES) - AN IMPORTANT TOOL TO ACCURATE DIAGNOSIS OF PRENATAL CONGENITAL ANOMALIES
    Castro, Lisandra
    Salgueiro, Natalia
    Conceicao, Ariana
    Moreira, Marta
    Garcia, Elsa
    Freitas, Michael
    Gavina, Adriana
    Alves, Claudia
    Correia, Cecilia
    Moldovan, Oana
    Lima, Margarida R.
    MEDICINE, 2025, 104 (04)
  • [40] Whole-exome sequencing of the patient with pyoderma gangrenosum
    Nesterovitch, A.
    Piontkivska, H.
    Hoffman, M.
    Mercer, H.
    Glant, T.
    Tharp, M.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2018, 138 (05) : S177 - S177