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Higher burden of rare frameshift indels in genes related to synaptic transmission separate familial hemiplegic migraine from common types of migraine.

Andreas Hoiberg RasmussenIsa OlofssonMona Ameri ChalmerJes OlesenThomas Folkmann Hansen
Published in: Journal of medical genetics (2020)
We show that patients with FHM compared with patients with common types of migraine suffer from a higher load of rare frameshift indels in genes associated with synaptic signalling in the central nervous system and possibly in muscle tissue contributing to vascular dysfunction.
Keyphrases
  • skeletal muscle
  • prefrontal cortex
  • oxidative stress
  • genome wide
  • early onset
  • risk factors
  • dna methylation
  • cerebrospinal fluid
  • bioinformatics analysis