Mutation in Glycerol-3-Phosphate Dehydrogenase 1–Like Gene (GPD1-L) Decreases Cardiac Na+ Current and Causes Inherited Arrhythmias

Overview of attention for article published in Circulation, October 2007

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French

Syndrome de Brugada

Cited by user BonifaceFR on 25 Jul 2022

Le syndrome de Brugada est une maladie génétique rare caractérisée par un sus-décalage du au niveau des dérivations précordiales droites V1, V2 et V3, et un aspect de…

English

GPD1L

Cited by user Boghog on 03 Sep 2008

GPD1L is a human gene. The protein encoded by this gene contains a glycerol-3-phosphate dehydrogenase (NAD+) motif and shares 72% sequence identity with GPD1.

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