Familial analysis reveals rare risk variants for migraine in regulatory regions.

Authors:
Techlo TR; Rasmussen AH; Møller PL; Bøttcher M; Winther S and 7 more

Journal:
Neurogenetics

Publication Year: 2020

DOI:
10.1007/s10048-020-00606-5

PMCID:
PMC7283211

PMID:
32076896

View on PubMed View on PMC View Publisher
Journal Information

Full Title: Neurogenetics

Abbreviation: Neurogenetics

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Neurology

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

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"Funding information The study was funded by a grant from Candys Foundation “CEHEAD”. The funding body was not involved in the design of the study and collection, analysis, and interpretation of data."

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