| Literature DB >> 10499169 |
E E Kors1, J Haan, M D Ferrari.
Abstract
Migraine has become an important topic in the field of complex genetic disorders. The identification of a gene on chromosome 19p encoding for an alpha 1A calcium channel subunit causing familial hemiplegic migraine has led to the classification of migraine as a channelopathy. More recently, efforts have been made to clarify the genetics of other primary headaches.Entities:
Mesh:
Year: 1999 PMID: 10499169 DOI: 10.1097/00019052-199906000-00002
Source DB: PubMed Journal: Curr Opin Neurol ISSN: 1350-7540 Impact factor: 5.710