Results 181 to 190 of about 10,273 (224)

Mechanistic Basis for Type 2 Long QT Syndrome Caused by KCNH2 Mutations that Disrupt Conserved Arginine Residues in the Voltage Sensor

open access: green, 2013
Christie M. McBride   +9 more
openalex   +1 more source

The Diagnostic Value of Copy Number Variants in Genetic Cardiomyopathies and Channelopathies. [PDF]

open access: yesJ Cardiovasc Dev Dis
Caputo V   +9 more
europepmc   +1 more source

The Uncommon Phenomenon of Short QT Syndrome: A Scoping Review of the Literature. [PDF]

open access: yesJ Pers Med
Boulmpou A   +8 more
europepmc   +1 more source

KCNH2 polymorphism in MMT Kelantanese Malay patients and QTc value-1.tab

open access: green, 2018
Muhammad Irfan Muslih AbdulKarim Ibrahim Nasir Mohamad Nurfadhlina Musa Rusli Ismail Zalina Zahari Abdul Jalal
openalex   +1 more source

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