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SNTA1 gene

Known as: dystrophin-associated protein A1, 59kDa, acidic component, SNTA1, TACIP1 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Rare variants in genes encoding the cardiac sodium channel and associated compounds and their impact on outcome of catheter ablation of atrial fibrillation
Aim Rare variants of genes encoding the cardiac sodium channel and associated compounds have been linked with atrial fibrillation… 
2015
2015
Targeted Gene Resequencing (Astrochip) to Explore the Tripartite Synapse in Autism–Epilepsy Phenotype with Macrocephaly
The frequent co-occurrence of autism spectrum disorders (ASD) and epilepsy, or paroxysmal EEG abnormalities, defines a condition… 
2012
2012
SYNERGISTIC EFFECT OF THE NOVEL MUTATIONS IN SCN5A AND SNTA1 ON LATE INA CONTRIBUTING TO LQT SYNDROME
Objectives SCN5A and SNTA1 are reported susceptible genes for long QT syndrome (LQTS). This study was designed to elucidate a… 
2002
2002
The intracellular microenvironment in host cell-specific phosphorylation of SNT1 by the FGFR1 tyrosine kinase.
The phosphorylation of the fibroblast growth factor receptor (FGFR) kinase substrate SNT1 (also called FGFR substrate 2, FRS2) by… 
Review
1997
Review
1997
Author's reply
In the December 2014 issue of Europace, Wong and Behr published a review on the role of undiagnosed inherited cardiac conditions… 
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