A β myosin heavy chain gene mutation causes restrictive cardiomyopathy

被引:0
|
作者
Jedeikin, R
Bensley, M
Hershberger, R
Rice, M
Reijo-Pera, R
Sehnert, A
机构
[1] Arizona Pediat Cardiol Consultants, Phoenix, AZ USA
[2] Univ Calif San Francisco, San Francisco, CA 94143 USA
[3] Oregon Hlth Sci Univ, Portland, OR 97201 USA
关键词
D O I
暂无
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
187
引用
收藏
页码:34A / 34A
页数:1
相关论文
共 50 条
  • [41] β-myosin heavy chain gene mutations in familial hypertrophic cardiomyopathy -: The usual suspect?
    McNally, EM
    CIRCULATION RESEARCH, 2002, 90 (03) : 246 - 247
  • [42] Two novel mutations in the β-myosin heavy chain gene associated with dilated cardiomyopathy
    Kärkkäinen, S
    Heliö, T
    Jääskeläinen, P
    Miettinen, R
    Tuomainen, P
    Ylitalo, K
    Kaartinen, M
    Reissell, E
    Toivonen, L
    Nieminen, MS
    Kuusisto, J
    Laakso, M
    Peuhkurinen, K
    EUROPEAN JOURNAL OF HEART FAILURE, 2004, 6 (07) : 861 - 868
  • [43] Allele-Specific Silencing Ameliorates Restrictive Cardiomyopathy Attributable to a Human Myosin Regulatory Light Chain Mutation
    Zaleta-Rivera, Kathia
    Dainis, Alexandra
    Ribeiro, Alexandre J. S.
    Cordero, Pablo
    Rubio, Gabriel
    Shang, Ching
    Liu, Jing
    Finsterbach, Thomas
    Parikh, Victoria N.
    Sutton, Shirley
    Seo, Kinya
    Sinha, Nikita
    Jain, Nikhil
    Huang, Yong
    Hajjar, Roger J.
    Kay, Mark A.
    Szczesna-Cordary, Danuta
    Pruitt, Beth L.
    Wheeler, Matthew T.
    Ashley, Euan A.
    CIRCULATION, 2019, 140 (09) : 765 - 778
  • [44] Double heterozygosity for a mutation in the β myosin heavy chain gene and in the cardiac myosin binding protein C gene in familial hypertrophic cardiomyopathy:: Phenotype-genotype relationship.
    Richard, P
    Isnard, R
    Dubourg, O
    Carrier, L
    Hagege, A
    Charron, P
    Bouhour, JB
    Hainque, B
    Schwartz, K
    Komajda, M
    CIRCULATION, 1998, 98 (17) : 506 - 507
  • [45] Novel Mutation in the α-Myosin Heavy Chain Gene Is Associated With Sick Sinus Syndrome
    Ishikawa, Taisuke
    Jou, Chuanchau J.
    Nogami, Akihiko
    Kowase, Shinya
    Arrington, Cammon B.
    Barnett, Spencer M.
    Harrell, Daniel T.
    Arimura, Takuro
    Tsuji, Yukiomi
    Kimura, Akinori
    Makita, Naomasa
    Circulation-Arrhythmia and Electrophysiology, 2015, 8 (02): : 400 - U200
  • [46] Mutation of perinatal myosin heavy chain - Reply
    Basson, CT
    Veugelers, M
    McDermott, DA
    NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (24): : 2557 - 2558
  • [47] Restrictive cardiomyopathy due to novel desmin gene mutation
    Ojrzynska, Natalia
    Bilinska, Zofia T.
    Franaszczyk, Maria
    Ploski, Rafal
    Grzybowski, Jacek
    KARDIOLOGIA POLSKA, 2017, 75 (07) : 723 - 723
  • [48] A MOLECULAR-BASIS FOR FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - A BETA-CARDIAC MYOSIN HEAVY-CHAIN GENE MISSENSE MUTATION
    GEISTERFERLOWRANCE, AAT
    KASS, S
    TANIGAWA, G
    VOSBERG, HP
    MCKENNA, W
    SEIDMAN, CE
    SEIDMAN, JG
    CELL, 1990, 62 (05) : 999 - 1006
  • [49] Homozygotes for a R869G mutation in the β-myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathy
    Richard, P
    Charron, P
    Leclercq, C
    Ledeuil, C
    Carrier, L
    Dubourg, O
    Desnos, M
    Bouhour, JB
    Schwartz, K
    Daubert, JC
    Komajda, M
    Hainque, B
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2000, 32 (08) : 1575 - 1583
  • [50] Identification of a novel missense mutation in the cardiac beta-myosin heavy chain gene in a Chinese patient with sporadic hypertrophic cardiomyopathy
    Kuang, SQ
    Yu, JD
    Lu, L
    He, LM
    Gong, LS
    Chen, SJ
    Chen, Z
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1996, 28 (09) : 1879 - 1883