Whole exome sequencing identifies novel genetic variants associated with syndromic Tetralogy of Fallot

被引：0
作者：
Toth-Szumutku, Fanni [1 ]
Kun, Ilona [1 ]
Lengyel, Anna [1 ]
Pinti, Eva [1 ]
Nemeth, Krisztina [1 ]
Abonyi, Tunde [1 ]
Ryu, Seung Woo [2 ]
Song, Yongjun [2 ]
Kis, Eva [3 ]
Ablonczy, Laszlo [3 ]
Goda, Vera [4 ]
Krivan, Gergely [4 ]
Haltrich, Iren [1 ]
Kovacs, Arpad Ferenc [1 ]
机构：
[1] Semmelweis Univ, Tuzolto St Dept, Pediat Ctr, Budapest, Hungary
[2] Billion Inc, Seoul, South Korea
[3] Gottsegen Natl Cardiovascular Ctr, Budapest, Hungary
[4] Natl Inst Hematol & Infect Dis, Cent Hosp Southern Pest, Budapest, Hungary
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P07.021.A
引用
收藏
页码：1392 / 1392
页数：1
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