Mutations In MYH7 Are Also Associated with Idiopathic Familial Restrictive Cardiomyopathy

被引：0
|
作者：
Khullar, Madhu [1 ]
Rai, Taranjit S. [1 ]
Bahl, Ajay [1 ]
Saikia, Uma N. [1 ]
Singh, Balvinder [2 ]
Talwar, Kewal [1 ]
机构：
[1] Postgrad Inst med Educ & Rsch, Chandigarh, India
[2] IMTECH, Chandigarh, India
来源：
CIRCULATION | 2008年 / 118卷 / 18期
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：S623 / S623
页数：1
相关论文
共 50 条
  • [41] MYH7 p.Glu903Gln Is a Pathogenic Variant Associated With Hypertrophic Cardiomyopathy
    Dias, Glauber M.
    Lamounier Junior, Arsonval
    Seifert, Maila
    Barajas-Martinez, Hector
    Barr, Daniel
    Sternick, Eduardo B.
    Medina-Acosta, Enrique
    Campos de Carvalho, Antonio C.
    Cruz Filho, Fernando E. S.
    CIRCULATION-GENOMIC AND PRECISION MEDICINE, 2021, 14 (05): : E003476
  • [42] Genetic variations of β-MYH7 in Venezuelan patients with hypertrophic cardiomyopathy.
    Rodriguez, Rosalva
    Guerrero, David
    Rivas, Yoyna
    Lacruz, Andrea
    Flores, Yris
    INVESTIGACION CLINICA, 2014, 55 (01): : 23 - 31
  • [43] A founder pathogenic variant in MYH7 causing hypertrophic cardiomyopathy in Catalonia
    Fernandez-Alvarez, P.
    Codina, M.
    Limeres, J.
    Serra-Juhe, C.
    Masas Castro, M.
    Cordero Lopez, A.
    Garcia-Arumi, E.
    Tizzano, E.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 278 - 279
  • [44] Scapuloperoneal Myopathy and Cardiomyopathy with a Novel MYH7 Mutation: A Case Report
    Hooshmand, Sara
    Govindarajan, Raghav
    NEUROLOGY, 2020, 94 (15)
  • [45] 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
  • [46] 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
  • [47] New Variant of MYH7 Gene Nucleotide Sequence in Familial Non-Compaction Cardiomyopathy with Benign Course
    Myasnikov, Roman P.
    Kulikova, Olga, V
    Meshkov, Alexey N.
    Kiseleva, Anna, V
    Shumarina, Anna O.
    Koretskiy, Sergey N.
    Zharikova, Anastasia A.
    Divashuk, Mikhail G.
    Kharlap, Maria S.
    Serduk, Svetlana E.
    Mershina, Elena A.
    Sinitsyn, Valentin E.
    Boytsov, Sergey A.
    Drapkina, Oxana M.
    RATIONAL PHARMACOTHERAPY IN CARDIOLOGY, 2020, 16 (03) : 383 - 391
  • [48] A MYH7 variant in a five-generation-family with hypertrophic cardiomyopathy
    Franke, Magda
    Ksiazczyk, Tomasz Marcin
    Dux, Marta
    Chmielewski, Przemyslaw
    Truszkowska, Grazyna
    Czapczak, Dorota
    Pietrzak, Radoslaw
    Bilinska, Zofia Teresa
    Demkow, Urszula
    Werner, Bozena
    FRONTIERS IN GENETICS, 2024, 15
  • [49] Inhibition of mTOR or MAPK ameliorates vmhcl/myh7 cardiomyopathy in zebrafish
    Bu, Haisong
    Ding, Yonghe
    Li, Jiarong
    Zhu, Ping
    Shih, Yu-Huan
    Wang, Mingmin
    Zhang, Yuji
    Lin, Xueying
    Xu, Xiaolei
    JCI INSIGHT, 2021, 6 (24)
  • [50] Severe hypertrophic cardiomyopathy in a patient with a homozygous MYH7 gene variant
    Serra, Walter
    Vitetta, Giulia
    Uliana, Vera
    Barocelli, Federico
    Barili, Valeria
    Allegri, Isabella
    Ardissino, Diego
    Gualandi, Francesca
    Percesepe, Antonio
    HELIYON, 2022, 8 (12)
12345