Significant linkage to migrane with aura on chromosome 11q24
Migraine with aura (MA) is a prevalent neurological condition with strong evidence for a genetic basis. Familial hemiplegic migraine, a rare Mendelian form of MA, can be caused by mutations in the calcium channel gene, CACNA1A or in the ATP1A2 gene, a Na+/K+ pump. Susceptibility genes for the more p...
Main Authors: | Cader, Z, Noble-Topham, S, Dyment, D, Cherny, S, Brown, J, Rice, G, Ebers, G |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2003
|
Similar Items
-
Significant linkage to migraine with aura on chromosome 11q24.
by: Cader, Z, et al.
Published: (2003) -
Genetic loading in familial migraine with aura.
by: Noble-Topham, SE, et al.
Published: (2003) -
Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13.
by: Noble-Topham, SE, et al.
Published: (2002) -
A genome-wide scan of 42 Canadian families suffering migraine with aura
by: Cader, M, et al.
Published: (2002) -
Chromosome 1p36 in migraine with aura: association study of the 5HT(1D) locus.
by: Thompson, MD, et al.
Published: (2012)