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ATP1A2 gene

Known as: ATP1A2, FHM2, ATPase Na+/K+ transporting subunit alpha 2 
National Institutes of Health

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ATP1A1 geneMIGRAINE, FAMILIAL HEMIPLEGIC, 2

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
A Chinese family with familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2
Background ATP1A2 has been identified as the genetic cause of familial hemiplegic migraine type 2. Over 80 ATP1A2 mutations have… 
2016
2016
Atp1a2 contributes modestly to alcohol-related behaviors.
2014
2014
Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci
Migraine headaches are a common comorbidity in Rolandic epilepsy (RE) and familial aggregation of migraine in RE families… 
2010
2010
Umbilical Cord Blood T Cells Respond against the Melan-A/MART-1 Tumor Antigen and Exhibit Reduced Alloreactivity as Compared with Adult Blood-Derived T Cells
Umbilical cord blood (UCB) is increasingly used as a source of hematopoietic progenitor cells to treat a variety of disorders… 
2007
2007
M - 7 Migraine hmiplgique familiale, pilepsie absence et ATP1A2
Highly Cited
2005
Highly Cited
2005
Familial basilar migraine associated with a new mutation in the ATP1A2 gene
Basilar migraine (BM), familial hemiplegic migraine (FHM), and sporadic hemiplegic migraine (SHM) are phenotypically similar… 
2005
2005
No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizures
2005
2005
A third Na+-binding site in the sodium pump.
The sodium pump, or Na,K-ATPase, exports three intracellular sodium ions in exchange for two extracellular potassium ions. In the… 
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