Oligogenic inheritance in long QT syndrome and hypertrophic cardiomyopathy

被引:0
|
作者
Dean, John [1 ]
Brown, C. [1 ]
Walker, D. [1 ]
Clark, C. [1 ]
Kelly, K. [1 ]
Broadhurst, P. [2 ]
Choy, A-M [3 ]
Lam, W. [4 ]
Murday, V. [5 ]
Goudie, D. [6 ]
Grieve, J. [7 ]
机构
[1] Univ Aberdeen, Dept Med Genet, Aberdeen AB9 1FX, Scotland
[2] Aberdeen Royal Infirm, Dept Cardiol, Aberdeen, Scotland
[3] Univ Dundee, Dept Cardiol, Dundee DD1 4HN, Scotland
[4] SE Scotland Reg Genet Serv, Edinburgh, Midlothian, Scotland
[5] Yorkhill Childrens Hosp, Dept Med Genet, Glasgow, Lanark, Scotland
[6] Ninewells Hosp, Dept Human Genet, Dundee DD1 9SY, Scotland
[7] Univ Aberdeen, Dept Forens Med, Aberdeen AB9 1FX, Scotland
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:S26 / S26
页数:1
相关论文
共 50 条
  • [41] Oligogenic inheritance in neuroblastoma
    Longo, L
    Tonini, GP
    Ceccherini, I
    Perri, P
    [J]. CANCER LETTERS, 2005, 228 (1-2) : 65 - 69
  • [42] Tako-tsubo cardiomyopathy and congenital long QT syndrome
    Squadroni, Liliana
    Di Matteo, Francisco
    Reisvig, Mariela L.
    Garmendia, Francisco
    Sanchez, Melisa
    Garcia, Maximiliano
    Guimaraenz, Marcelo
    Estebanez, Maria J.
    Montovani, Adriana
    De Feo, Fernando
    [J]. INSUFICIENCIA CARDIACA, 2019, 14 (04) : 154 - 157
  • [43] A CONGENITAL DEADLY ASSOCIATION: DILATED CARDIOMYOPATHY AND LONG QT SYNDROME
    Lima, Neiberg de Alcantara
    Shamsi, Wasif Elahi
    Andrade, Antonio Thomaz
    Sampaio, Stela
    De Castro, Ricardo
    Lima, Carol
    Loehrke, Mark
    [J]. CHEST, 2020, 158 (04) : 242A - 242A
  • [44] A Potential Oligogenic Etiology of Hypertrophic Cardiomyopathy A Classic Single-Gene Disorder
    Li, Lili
    Bainbridge, Matthew Neil
    Tan, Yanli
    Willerson, James T.
    Marian, Ali J.
    [J]. CIRCULATION RESEARCH, 2017, 120 (07) : 1084 - +
  • [45] The mutational burden and oligogenic inheritance in Klippel-Feil syndrome
    Ziquan Li
    Sen Zhao
    Siyi Cai
    Yuanqiang Zhang
    Lianlei Wang
    Yuchen Niu
    Xiaoxin Li
    Jianhua Hu
    Jingdan Chen
    Shengru Wang
    Huizi Wang
    Gang Liu
    Ye Tian
    Zhihong Wu
    Terry Jianguo Zhang
    Yipeng Wang
    Nan Wu
    [J]. BMC Musculoskeletal Disorders, 21
  • [46] GENOMIC IMPRINTING IN THE INHERITANCE OF FAMILIAL HYPERTROPHIC CARDIOMYOPATHY
    ELSTEIN, E
    CLARKE, LA
    RAKOWSKI, H
    PERRYMAN, MB
    ROBERTS, R
    WIGLE, ED
    HAYDEN, MR
    SOLE, MJ
    [J]. CIRCULATION, 1992, 86 (04) : 272 - 272
  • [47] The mutational burden and oligogenic inheritance in Klippel-Feil syndrome
    Li, Ziquan
    Zhao, Sen
    Cai, Siyi
    Zhang, Yuanqiang
    Wang, Lianlei
    Niu, Yuchen
    Li, Xiaoxin
    Hu, Jianhua
    Chen, Jingdan
    Wang, Shengru
    Wang, Huizi
    Liu, Gang
    Tian, Ye
    Wu, Zhihong
    Zhang, Terry Jianguo
    Wang, Yipeng
    Wu, Nan
    [J]. BMC MUSCULOSKELETAL DISORDERS, 2020, 21 (01)
  • [48] Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family
    Ichikawa, Mari
    Ohno, Seiko
    Fujii, Yusuke
    Ozawa, Junichi
    Sonoda, Keiko
    Fukuyama, Megumi
    Kato, Koichi
    Kimura, Hiromi
    Itoh, Hideki
    Hayashi, Hideki
    Horie, Minoru
    [J]. INTERNAL MEDICINE, 2016, 55 (03) : 259 - 262
  • [49] Syndactyly and long QT syndrome (Cav1.2 missense mutation G406R) is associated with hypertrophic cardiomyopathy
    Lo-A-Njoe, SM
    Wilde, AA
    van Erven, L
    Blom, NA
    [J]. HEART RHYTHM, 2005, 2 (12) : 1365 - 1368
  • [50] Cardiac conduction system anomalies in fetal and adult hearts of a transgenic model of Long QT-Syndrome associate to hypertrophic cardiomyopathy
    De La Rosa Sanchez, A. J.
    Dominguez, J.
    Sedmera, D.
    Franco, D.
    Aranega, A.
    [J]. CARDIOVASCULAR RESEARCH, 2010, 87 : S122 - S122