Non-Syndromic Mitral Valve Prolapse From Gene Mutations to Modifiable Mechanisms

被引：0
|
作者：
Norris, Russell
Sauls, Kimberly
Durst, Ronen
Peal, David
Toomer, Katelynn
Leyne, Maire
Talkowski, Michael E.
Brand, Harrison
Perrocheau, Maelle
Lynch, Stacey N.
Bouaia-Naji, Nabila
Delling, Francesca N.
Freed, Lisa A.
Le Tourneau, Thierry
LeMarec, Herve
Estivill, Xavier
Fernandez-Friera, Leticia
Dina, Christian
Solis, Jorge
Trujillano, Daniel
Irvine, Kenneth D.
Mao, Yaopan
Ossowski, Stephan
Wessels, Any
Menick, Donald
Kasiganesan, Harinath
Bromme, Ann-Marie
Williams, Katherine
Schott, Jean-Jacques
Hagege, Albert A.
Jeunemaitre, Xavier
Markwald, Roger R.
Milan, David J.
Levine, Robert A.
Slaugenhaupt, Susan
机构：
来源：
CIRCULATION | 2014年 / 130卷
关键词：
Mitrel valve disease; Electrocardiography;
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
18977
引用
收藏
页数：5
相关论文
共 50 条
  • [31] Mitochondrial mutations in non-syndromic hearing loss at UAE
    Mohamed, Walaa Kamal Eldin
    Arnoux, Marc
    Cardoso, Thyago H. S.
    Almutery, Abdullah
    Tlili, Abdelaziz
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2020, 138
  • [32] Connexin 26 Gene Mutations in Non-Syndromic Hearing Loss Among Kuwaiti Patients
    Al-Sebeih, Khalid
    Al-Kandari, Marium
    Al-Awadi, Sadika A.
    Hegazy, Fatma F.
    Al-Khamees, Ghada A.
    Naguib, Kamal K.
    Al-Dabbous, Reem M.
    MEDICAL PRINCIPLES AND PRACTICE, 2014, 23 (01) : 74 - 79
  • [33] Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene
    Aldrees, Alanoud
    Abdelkader, Ehab
    Al-Habboubi, Hussain
    Alrwebah, Huda
    Rahbeeni, Zuhair
    Schatz, Patrik
    OPHTHALMIC GENETICS, 2019, 40 (01) : 77 - 79
  • [34] Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment
    Verhoeven, K
    Van Laer, L
    Kirschhofer, K
    Legan, PK
    Hughes, DC
    Schatteman, I
    Verstreken, M
    Van Hauwe, P
    Coucke, P
    Chen, A
    Smith, RJH
    Somers, T
    Offeciers, FE
    Van de Heyning, P
    Richardson, GP
    Wachtler, F
    Kimberling, WT
    Willems, PJ
    Govaerts, PJ
    Van Camp, G
    NATURE GENETICS, 1998, 19 (01) : 60 - 62
  • [35] Screening for mutations in the connexin 31 gene in Brazilian patients with non-syndromic deafness.
    Sartorato, EL
    Alexandrino, F
    Oliveira, CA
    Maciel-Guerra, AT
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 563 - 563
  • [36] Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia
    Wong, Singwai
    Liu, Haochen
    Bai, Baojing
    Chang, Huaiguang
    Zhao, Hongshan
    Wang, Yixiang
    Han, Dong
    Feng, Hailan
    ARCHIVES OF ORAL BIOLOGY, 2014, 59 (03) : 349 - 353
  • [37] Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment
    Kristien Verhoeven
    Lut Van Laer
    Karin Kirschhofer
    P. Kevin Legan
    David C. Hughes
    Isabelle Schatteman
    Margriet Verstreken
    Peter Van Hauwe
    Paul Coucke
    Achih Chen
    Richard J.H. Smith
    Thomas Somers
    F. Erwin Offeciers
    Paul Van de Heyning
    Guy P. Richardson
    Franz Wachtler
    William J. Kimberling
    Patrick J. Willems
    Paul J. Govaerts
    Guy Van Camp
    Nature Genetics, 1998, 19 : 60 - 62
  • [38] Ischemic mitral valve prolapse: mechanisms and implications for valve repair
    Jouan, J
    Tapia, M
    Cook, RC
    Lansac, E
    Acar, C
    EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2004, 26 (06) : 1112 - 1117
  • [39] Syndromic and non-syndromic disease-linked Cx43 mutations
    Laird, Dale W.
    FEBS LETTERS, 2014, 588 (08) : 1339 - 1348
  • [40] Molecular studies on ARX gene in syndromic and non-syndromic mental retardation
    Gayatri Kulkarni
    Suvidya Ranade
    Molecular Cytogenetics, 7 (Suppl 1)
12345