Same MYH7 gene mutation but different phenotypes of cardiomyopathy in one family

被引：0
|
作者：
Liu, Ting [1 ]
Yao, Yuan [1 ,2 ,3 ]
Kang, Yu [1 ]
Zhang, Qing [1 ,4 ]
机构：
[1] Sichuan Univ, West China Hosp, Dept Cardiol, Chengdu, Peoples R China
[2] West China Sch Publ Hlth, Dept Geriatr Med & Cardiol, Chengdu, Peoples R China
[3] West China Fourth Hosp, Chengdu, Peoples R China
[4] Sichuan Univ, West China Hosp, Dept Cardiol, 37 Guoxue St, Chengdu 610041, Peoples R China
来源：
KAOHSIUNG JOURNAL OF MEDICAL SCIENCES | 2023年 / 39卷 / 10期
关键词：
D O I：
10.1002/kjm2.12741
中图分类号：
R-3 [医学研究方法]; R3 [基础医学];
学科分类号：
1001 ;
摘要：
引用
收藏
页码：1052 / 1053
页数：2
相关论文
共 50 条
  • [1] A Family with Myh7 Mutation and Different Forms of Cardiomyopathies
    Catrina, Bianca Iulia
    Batar, Florina
    Baltat, Georgiana
    Bitea, Cornel Ioan
    Puia, Andreea
    Stoia, Oana
    Fleaca, Sorin Radu
    Teodoru, Minodora
    BIOMEDICINES, 2023, 11 (07)
  • [2] A novel mutation of the MYH7 gene in a patient with hypertrophic cardiomyopathy
    Goel, Nicholas
    Huddleston, Charles B.
    Fiore, Andrew C.
    TURKISH JOURNAL OF PEDIATRICS, 2018, 60 (03) : 315 - 318
  • [3] Novel mutation in MYH7 gene associated with distal myopathy and cardiomyopathy
    Homayoun, Houman
    Khavandgar, Simin
    Hoover, Jacqueline M.
    Mohsen, Al-Walid
    Vockley, Jerry
    Lacomis, David
    Clemens, Paula R.
    NEUROMUSCULAR DISORDERS, 2011, 21 (03) : 219 - 222
  • [4] MYH7 mutation associated with two phenotypes of myopathy
    Li, Nan
    Zhao, Zhe
    Shen, Hongrui
    Bing, Qi
    Guo, Xuan
    Hu, Jing
    NEUROLOGICAL SCIENCES, 2018, 39 (02) : 333 - 339
  • [5] MYH7 mutation associated with two phenotypes of myopathy
    Nan Li
    Zhe Zhao
    Hongrui Shen
    Qi Bing
    Xuan Guo
    Jing Hu
    Neurological Sciences, 2018, 39 : 333 - 339
  • [6] Screening of MYH7 gene mutation sites in hypertrophic cardiomyopathy and its significance
    Liu, Hui-Ting
    Ji, Fang-Fang
    Wei, Ling
    Zuo, An-Jun
    Gao, Yu-Xiu
    Qi, Lin
    Jin, Bu
    Wang, Ji-Gang
    Zhao, Peng
    CHINESE MEDICAL JOURNAL, 2019, 132 (23) : 2835 - 2841
  • [7] Screening of MYH7 gene mutation sites in hypertrophic cardiomyopathy and its significance
    Liu Hui-Ting
    Ji Fang-Fang
    Wei Ling
    Zuo An-Jun
    Gao Yu-Xiu
    Qi Lin
    Jin Bu
    Wang Ji-Gang
    Zhao Peng
    中华医学杂志英文版, 2019, 132 (23) : 2835 - 2841
  • [8] A novel mutation in MYH7 giving rise to different phenotypes in a mother and her daughter
    Orstavik, K.
    Almaas, V.
    Rasmussen, M.
    Jonsrud, C.
    Jensen, S.
    Loseth, S.
    Leren, T.
    NEUROMUSCULAR DISORDERS, 2018, 28 : S107 - S107
  • [9] New Genetic Variant in the MYH7 Gene Associated With Hypoplastic Right Heart Syndrome and Hypertrophic Cardiomyopathy in the Same Family
    Polyakova, Elizaveta
    van Gils, Janine M.
    Stoeger, J. Lauran
    Kies, Philippine
    Egorova, Anastasia D.
    Koopmann, Tamara T.
    van Dijk, Tessa
    Deruiter, Marco C.
    Barge-Schaapveld, Daniela Q. C. M.
    Jongbloed, Monique R. M.
    CIRCULATION-GENOMIC AND PRECISION MEDICINE, 2023, 16 (06): : E004184
  • [10] Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation
    Overeem, S.
    Schelhaas, H. J.
    Blijham, P. J.
    Grootscholten, M. I.
    ter Laak, H. J.
    Timmermans, J.
    van den Wijngaard, A.
    Zwarts, M. J.
    NEUROMUSCULAR DISORDERS, 2007, 17 (06) : 490 - 493
12345