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. 2020 Jan 24;57(9):610–616. doi: 10.1136/jmedgenet-2019-106640

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© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

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(A) Bar plot of gene fold change enrichment of the 28 genes, which had significantly more frameshift indels in FHM compared with Fam. migraine in 23 human tissues from the GTEx RNA-seq database. (B) Bar plot of gene fold change enrichment of the 92 genes, which had significantly more frameshift indels in FHM compared with Spo. migraine in 23 human tissues from the GTEx RNA-seq database. All asterisks display the significance level (padj<0.05). Fam., familial; FHM, familial hemiplegic migraine; Spo., sporadic.