Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred

We sought to map the disease-causing gene in a large Spanish kindred with familial hemiplegic migraine (FHM). Patients were classified according to the ICHD-II criteria. After ruling out linkage to known migraine genetic loci, a single nucleotide polymorphism-based, 0.62-cM density genome-wide scan...

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Veröffentlicht in:	Neurogenetics 2009-07, Vol.10 (3), p.191-198
Hauptverfasser:	Cuenca-León, Ester, Corominas, Roser, Montfort, Magda, Artigas, Josep, Roig, Manuel, Bayés, Mònica, Cormand, Bru, Macaya, Alfons
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Biological and medical sciences Biomedical and Life Sciences Biomedicine Child Child, Preschool Chromosomes, Human, Pair 14 Classical genetics, quantitative genetics, hybrids DNA Mutational Analysis Female Fundamental and applied biological sciences. Psychology Genetic disorders Genetic Heterogeneity Genetic Linkage Genetic Predisposition to Disease Genetics of eukaryotes. Biological and molecular evolution Genome, Human Genome-Wide Association Study Genotype & phenotype Human Human Genetics Humans Lod Score Male Migraine Migraine with Aura - genetics Molecular and cellular biology Molecular Medicine Neurosciences Original Article Pedigree Polymorphism Polymorphism, Single Nucleotide Spain Vertebrates: nervous system and sense organs
Online-Zugang:	Volltext
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