Two novel mutations, two different clinical phenotypes associated with SCN5A; Brugada and Long QT syndromes

被引：0
|
作者：
Peker, Alp [1 ]
Toylu, Asli [1 ]
Coskun, Mert [1 ]
Karamik, Gokcen [2 ]
Altunbas, Feyza [1 ]
Araci, Duygu Gamze [1 ]
Ozturk, Nuray [2 ]
Nur, Banu [2 ]
Yildirim, Aytul Belgi [3 ]
Ekici, Filiz [4 ]
Clark, Ozden Altiok [1 ]
Mihci, Ercan [2 ]
机构：
[1] Akdeniz Univ, Med Genet, Sch Med, Antalya, Turkiye
[2] Akdeniz Univ, Pediat Genet, Sch Med, Antalya, Turkiye
[3] Akdeniz Univ, Cardiol, Sch Med, Antalya, Turkiye
[4] Akdeniz Univ, Pediat Cardiol, Sch Med, Antalya, Turkiye
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31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：
EP06.034
引用
收藏
页码：145 / 145
页数：1
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