Congenital Long QT Syndrome Genes (KCNQ1, KCNH2, SCN5A)

Từ khóa » Kcnh2 Long Qt

• Characterization Of Novel KCNH2 Mutations In Type 2 Long QT ...

• Characterization Of Novel KCNH2 Mutations In Type 2 Long QT ... - NCBI

• Common Genetic Variation In KCNH2 Is Associated With QT Interval ...

• An Actionable KCNH2 Long QT Syndrome Variant Detected By ...

• A Novel KCNH2 Frameshift Mutation (c.46delG) Associated With High ...

• Heterogeneous Phenotype Of Long QT Syndrome Caused By The ...

• Long QT Syndrome Type 2: Emerging Strategies For Correcting ...

• Contribution Of A KCNH2 Variant In Genotyped Long QT Syndrome

• Entry - #613688 - LONG QT SYNDROME 2; LQT2 - OMIM

• Long QT Syndrome With Nocturnal Cardiac Events Caused ... - J-Stage

• Novel Mutation In The KCNH2 Gene Associated With Long QT Syndrome

• Discovery Of Digenic Mutation, KCNH2 C.1898A >C And JUP C ...

• Diagnosis, Management And Therapeutic Strategies For Congenital ...