Analysis of a family with brugada syndrome and sudden cardiac death caused by a novel mutation of SCN5A
YB Zhu, JH Zhang, YY Ji, YN Hu… - Cardiology …, 2022 - Wiley Online Library
Background. Brugada syndrome is a hereditary cardiac disease associated with mutations
in ion channel genes. The clinical features include ventricular fibrillation, syncope, and …
in ion channel genes. The clinical features include ventricular fibrillation, syncope, and …
[HTML][HTML] Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A
YB Zhu, JH Zhang, YY Ji, YN Hu, HL Wang… - Cardiology Research …, 2022 - ncbi.nlm.nih.gov
Background Brugada syndrome is a hereditary cardiac disease associated with mutations in
ion channel genes. The clinical features include ventricular fibrillation, syncope, and sudden …
ion channel genes. The clinical features include ventricular fibrillation, syncope, and sudden …
Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A.
YB Zhu, JH Zhang, YY Ji, YN Hu… - Cardiology …, 2022 - search.ebscohost.com
Background. Brugada syndrome is a hereditary cardiac disease associated with mutations
in ion channel genes. The clinical features include ventricular fibrillation, syncope, and …
in ion channel genes. The clinical features include ventricular fibrillation, syncope, and …
Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A
YB Zhu, JH Zhang, YY Ji, YN Hu… - Cardiology …, 2022 - pubmed.ncbi.nlm.nih.gov
Background Brugada syndrome is a hereditary cardiac disease associated with mutations in
ion channel genes. The clinical features include ventricular fibrillation, syncope, and sudden …
ion channel genes. The clinical features include ventricular fibrillation, syncope, and sudden …
[PDF][PDF] Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A
YB Zhu, JH Zhang, YY Ji, YN Hu, HL Wang, DD Ruan… - 2022 - scienceopen.com
Background. Brugada syndrome is a hereditary cardiac disease associated with mutations
in ion channel genes. e clinical features include ventricular fibrillation, syncope, and sudden …
in ion channel genes. e clinical features include ventricular fibrillation, syncope, and sudden …
Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A.
YB Zhu, JH Zhang, YY Ji, YN Hu, HL Wang… - Cardiology Research …, 2022 - europepmc.org
Background Brugada syndrome is a hereditary cardiac disease associated with mutations in
ion channel genes. The clinical features include ventricular fibrillation, syncope, and sudden …
ion channel genes. The clinical features include ventricular fibrillation, syncope, and sudden …
Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A
Z Yao-Bin, Z Jian-Hui, J Yuan-Yuan… - Cardiology …, 2022 - search.proquest.com
Background. Brugada syndrome is a hereditary cardiac disease associated with mutations
in ion channel genes. The clinical features include ventricular fibrillation, syncope, and …
in ion channel genes. The clinical features include ventricular fibrillation, syncope, and …
Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A.
YB Zhu, JH Zhang, YY Ji, YN Hu, HL Wang… - … Research and Practice, 2022 - go.gale.com
Background. Brugada syndrome is a hereditary cardiac disease associated with mutations
in ion channel genes. The clinical features include ventricular fibrillation, syncope, and …
in ion channel genes. The clinical features include ventricular fibrillation, syncope, and …