IndraLab

Statements

CACNA1A activates Migraine with Aura. 5 / 6
| 5
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"FHM1 and SHM1 is a rare migraine with an aura subtype caused by CACNA1A variants, which is characterized by hemiparesis and occasionally encephalopathy during migraine attacks."
33425808
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"Missense mutation R192Q in the CACNA1A gene causes familial hemiplegic migraine type-1 (FHM1), a monogenic subtype of migraine with aura."
24583041
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"Familial Hemiplegic Migraine type 1 (FHM1) is a rare monogenic subtype of migraine with aura caused by mutations in the CACNA1A gene."
| PMC
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"Familial hemiplegic migraine type 1 (FHM1) is a rare monogenic subtype of migraine with aura caused by mutations in CACNA1A that encodes the alpha 1A subunit of voltage gated Ca V 2.1 calcium channels."
27032388
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"Familial hemiplegic migraine type 1 (FHM1), a severe migraine with aura variant, is caused by mutations in the CACNA1A gene."
37277733