Abstract
To determine the extent to which mutations in genes known to cause familial hemiplegic migraine (FHM) account for the disorder, the authors used a population-based approach through the Danish National Patient Register. In members of 42 families with FHM, they sequenced the exon and promoter regions of the CACNA1A and ATP1A2 genes. They also sought the Q1489K mutation in the SCN1A gene. Mutations …
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
