[HTML][HTML] Studying Brugada syndrome with an SCN1B variants in human-induced pluripotent stem cell-derived cardiomyocytes
Background Among rare channelopathies BrS patients are at high risk of sudden cardiac
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes
I El-Battrawy, J Müller, Z Zhao, L Cyganek, R Zhong… - 2019 - agris.fao.org
BackgroundAmong rare channelopathies BrS patients are at high risk of sudden cardiac
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
Studying Brugada syndrome with an SCN1B variants in human-induced pluripotent stem cell-derived cardiomyocytes
I El-Battrawy, J Müller, Z Zhao… - Frontiers in Cell and …, 2019 - edoc.mdc-berlin.de
BACKGROUND: Among rare channelopathies BrS patients are at high risk of sudden
cardiac death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene …
cardiac death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene …
[HTML][HTML] Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes
I El-Battrawy, J Müller, Z Zhao, L Cyganek… - Frontiers in Cell and …, 2019 - ncbi.nlm.nih.gov
Background Among rare channelopathies BrS patients are at high risk of sudden cardiac
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
I El-Battrawy, J Müller, Z Zhao, L Cyganek… - Frontiers in Cell and …, 2019 - europepmc.org
Background Among rare channelopathies BrS patients are at high risk of sudden cardiac
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
[PDF][PDF] Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes
M Ponz-Sarvise, XC Vergara, HB Martinez, X Zhou… - core.ac.uk
Background: Among rare channelopathies BrS patients are at high risk of sudden cardiac
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes
I El-Battrawy, J Müller, Z Zhao… - Frontiers in cell …, 2019 - pubmed.ncbi.nlm.nih.gov
Background Among rare channelopathies BrS patients are at high risk of sudden cardiac
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes
I El-Battrawy, J Müller, Z Zhao, L Cyganek… - 2019 - publications.goettingen-research …
Background Among rare channelopathies BrS patients are at high risk of sudden cardiac
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
I El-Battrawy, J Müller, Z Zhao, L Cyganek… - Frontiers in Cell and …, 2019 - europepmc.org
Background Among rare channelopathies BrS patients are at high risk of sudden cardiac
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
[PDF][PDF] Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes
M Ponz-Sarvise, XC Vergara, HB Martinez, X Zhou… - edoc.mdc-berlin.de
Background: Among rare channelopathies BrS patients are at high risk of sudden cardiac
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …
death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations …