NKX2.5 mutations in patients with congenital heart disease (CHD)

被引：0
|
作者：
McElhinney, DB
Geiger, E
Blinder, J
Benson, DW
Goldmuntz, E
机构：
[1] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[2] Childrens Hosp, Med Ctr, Cincinnati, OH 45229 USA
来源：
CIRCULATION | 2002年 / 106卷 / 19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：
836
引用
收藏
页码：166 / 167
页数：2
相关论文
共 50 条
  • [1] NKX2.5 mutations in patients with congenital heart disease
    McElhinney, DB
    Geiger, E
    Blinder, J
    Benson, DW
    Goldmuntz, E
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2003, 42 (09) : 1650 - 1655
  • [2] NKX2.5 mutations in patients with non-syndromic congenital heart disease
    Gioli-Pereira, Luciana
    Pereira, Alexandre Costa
    Mesquita, Sonia M.
    Xavier-Neto, Jose
    Lopes, Antonio Augusto
    Krieger, Jose Eduardo
    [J]. INTERNATIONAL JOURNAL OF CARDIOLOGY, 2010, 138 (03) : 261 - 265
  • [3] NKX2.5 mutations and congenital heart disease: Is it a marker of cardiac anomalies?
    Balci, Mustafa M.
    Akdemir, Ramazan
    [J]. INTERNATIONAL JOURNAL OF CARDIOLOGY, 2011, 147 (03) : E44 - E45
  • [4] NKX2.5 mutation frequency in patients with congenital heart disease
    Gioli-Pereira, L.
    Pereira, A.
    Mesquita, S.
    Xavier-Neto, J.
    Lopes, A. A.
    Krieger, J. E.
    [J]. EUROPEAN HEART JOURNAL, 2006, 27 : 956 - 956
  • [5] Functional analyses of CSX/NKX2.5 mutations that cause human congenital heart disease
    Zhu, W
    Shiojima, I
    Oka, T
    Monzen, K
    Hiroi, Y
    Hosoda, T
    Zou, Y
    Komuro, I
    [J]. CIRCULATION, 2000, 102 (18) : 359 - 359
  • [6] Mutations of NKX2.5 and GATA4 genes in the development of congenital heart disease
    Tong, Yi-Fan
    [J]. GENE, 2016, 588 (01) : 86 - 94
  • [7] Functional analysis of the mutated Csx/Nkx2.5 in patients with a congenital heart disease
    Kasahara, H
    Lee, B
    Schott, JJ
    Benson, DW
    Seidman, JG
    Seidman, CE
    Izumo, S
    [J]. CIRCULATION, 1999, 100 (18) : 354 - 354
  • [8] Novel Point Mutations in the NKX2.5 Gene in Pediatric Patients with Non-Familial Congenital Heart Disease
    Khatami, Mehri
    Mazidi, Mansoureh
    Taher, Shabnam
    Heidari, Mohammad Mehdi
    Hadadzadeh, Mehdi
    [J]. MEDICINA-LITHUANIA, 2018, 54 (03):
  • [9] Investigation of NKX2.5 Gene Mutations in Congenital Heart Defects in an Indian Population
    Ketharnathan, Sarada
    Koshy, Teena
    Sethuratnam, Rajan
    Paul, Solomon
    Venkatesan, Vettriselvi
    [J]. GENETIC TESTING AND MOLECULAR BIOMARKERS, 2015, 19 (10) : 579 - 583
  • [10] NKX2.5 mutations in patients with tetralogy of Fallot
    Goldmuntz, E
    Geiger, E
    Benson, DW
    [J]. CIRCULATION, 2001, 104 (21) : 2565 - 2568
12345