Familial typical migraine : linkage to chromosome 19p13 and evidence for genetic heterogeneity

Migraine is a frequent familial disorder that, in common with most multifactorial disorders, has an unknown etiology. The authors identified several families with multiple individuals affected by typical migraine using a single set of diagnostic criteria and studied these families for cosegregation...

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Veröffentlicht in:	Neurology 1998-05, Vol.50 (5), p.1428-1432
Hauptverfasser:	NYHOLT, D. R, LEA, R. A, GOADSBY, P. J, BRIMAGE, P. J, GRIFFITHS, L. R
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Calcium Channels - genetics Chromosomes, Human, Pair 19 Female Genetic Heterogeneity Genetic Linkage Humans Lod Score Male Medical sciences Microsatellite Repeats Migraine Disorders - genetics Neurology Pedigree Software Statistics, Nonparametric Vascular diseases and vascular malformations of the nervous system
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