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Publications by Eija Hämäläinen
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families
Neuron
Neuroscience
The Contribution of CACNA1A, ATP1A2 and SCN1A Mutations in Hemiplegic Migraine: A Clinical and Genetic Study in Finnish Migraine Families
Cephalalgia
Medicine
Neurology
Pitfalls in Genetic Testing: The Story of missedSCN1Amutations
Molecular genetics & genomic medicine
Genetics
Molecular Biology