Work

The novel p.L1649Q mutation in theSCN1Aepilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies

Year: 2007

Type: article

Study design: Observational Study

Source: Human Mutation

DOI: 10.1002/humu.9486

Authors: Kaate R.J. Vanmolkot, Elena Babini, Boukje de Vries, Anine H. Stam, Tobias Freilinger, Gisela M. Terwindt, Lisa Norris, Joost Haan, Rune R. Frants, Nabih M. Ramadan, Michel D. Ferrari, Michael Pusch, Arn M.J.M. van den Maagdenberg, Martin Dichgans

Institutions: Leiden University Medical Center, University of Genoa, Ludwig-Maximilians-Universität München, Rosalind Franklin University of Medicine and Science, Rijnland Ziekenhuis

Language: English

Topic: Migraine and Headache Studies

Subfield: Psychiatry and Mental health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2016307898

FWCI: 8.641

Cites:

Cited by: 105

Related to: 10