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CACNA1A activates Familial Hemiplegic Migraine. 1 / 1

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"Stroke like episodes (SLE) occur in phosphomannomutase deficiency (PMM2-CDG), and may complicate the course of channelopathies related to Familial Hemiplegic Migraine (FHM) caused by mutations in CACNA1A (encoding Ca V 2.1 channel)."

29470411

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IndraLab

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CACNA1A activates Familial Hemiplegic Migraine. 1 / 1

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