The novel p.L1649Q mutation in theSCN1Aepilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies
Open Access
- 30 March 2007
- journal article
- mutation in-brief
- Published by Hindawi Limited in Human Mutation
- Vol. 28 (5), 522
- https://doi.org/10.1002/humu.9486