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Corrigendum to “Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant” Seizure 25 (2015) 65–67

机译：更正“在具有KCNQ1致病变异的家庭中LQT综合征与癫痫之间关联的更多证据” 癫痫发作25（2015）65-67

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Tiron Coloma; Campuzano Oscar; Pérez-Serra Alexandra; Mademont Irene; Coll Monica; Allegue Catarina; Iglesias Anna; Partemi Sara; Striano Pasquale; Oliva Antonio; Brugada Ramon;
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1. Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant (vol 25, pg 65, 2015) [J] . Tiron Coloma, Campuzano Oscar, Perez-Serra Alexandra, Seizure: the journal of the British Epilepsy Association . 2015,第Null期

机译：LQT综合征与KCNQ1致病变异性家庭癫痫之间关联的进一步证据（2015年第25卷，第65页）
2. Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant [J] . Tiron de Llano Coloma, Campuzano Oscar, Perez-Serra Alexandra, Seizure: the journal of the British Epilepsy Association . 2015,第Null期

机译：LQT综合征与KCNQ1致病变异家庭中癫痫之间关联的进一步证据
3. New onset seizures in a patient with Long QT Syndrome (LQTS2) and a pathogenic carboxyl-terminus frameshift variant of the KCNH2 gene [J] . Zarroli Katherine, Querfurth Henry Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia . 2018,第期

机译：新的QT综合征（LQTS2）的患者癫痫发作和KCNH2基因的致病性羧基末端的致病性羧基末端变体
4. Linkage Evidence for a Two-Locus Inheritance of LQT-Associated Seizures in a Multigenerational LQT Family With a Novel KCNQ1 Loss-of-Function Mutation [O] . Harald Prüss, Guido Gessner, Stefan H. Heinemann, 2019

机译：具有新型KCNQ1功能丧失突变的多代LQT家族中与LQT相关的癫痫发作的两基因座遗传连锁证据
5. Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant [O] . De Llano, Ct, Campuzano, O, Pérez-Serra, A, 2015

机译：LQT综合征与KCNQ1致病变异家庭中癫痫之间关联的进一步证据

Corrigendum to “Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant” Seizure 25 (2015) 65–67

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