Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity

Annals of Neurology

Volumn 42, Issue 6, 1997, Pages 885-890

  Ducros, Anne ^a   Joutel, Anne ^a   Vahedi, Katayoun ^b   Cecillon, Michaëlle ^a   Ferreira, Antonio ^c   Bernard, Evelyne ^c   Verier, Albert ^c   Echenne, Bernard ^d   De Munain, Adolfo Lopez ^e   Bousser, Marie Germaine ^b   Tournier Lasserve, Elisabeth ^a  

^a INSERM   (France)

^b HÔPITAL LARIBOISIÈRE   (France)

^c Hopital Schaffner   (France)

^d HÔPITAL SAINT ELOI   (France)

^e Hospital Nuestra Senora de Aranzazu   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CEREBELLAR ATAXIA; CHROMOSOME 19P; CHROMOSOME 1Q; DISEASE ASSOCIATION; FEMALE; GENE LOCATION; GENE LOCUS; GENE MUTATION; GENETIC HETEROGENEITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MIGRAINE; PEDIGREE ANALYSIS; PRIORITY JOURNAL;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 19; FEMALE; FRANCE; GENETIC HETEROGENEITY; HEMIPLEGIA; HUMANS; LINKAGE (GENETICS); MALE; MICROSATELLITE REPEATS; MIGRAINE DISORDERS; PEDIGREE;

EID: 0031470730     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410420610     Document Type: Article

References (25)

1. Headache Classification Committee of the International Headache Society. Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Cephalalgia 1988; 8(suppl 7):19-28
2. Whitty CWM. Familial hemiplegic migraine. J Neurol Neurosurg Psychiatry 1953;16:172-177
3. Blau JN, Whitty CWM. Familial hemiplegic migraine. Lancet 1955;2:1115-1116
4. Fitzimons RB, Wolfenden WH. Migraine coma. Meningitic migraine with cerebral oedema associated with a new form of autosomal dominant cerebellar ataxia. Brain 1985;108:555-577
5. Münte TF, Müller-Vahl H. Familial migraine coma: a case study. J Neurol 1990;237:59-61
6. Ohta M, Araki S, Kuroiwa Y. Familial occurrence of migraine with an hemiplegic syndrome and cerebellar manifestations. Neurology 1967;17:813-817
7. Codina A, Acarini PN, Miguel F. Migraine hémiplégique associée à un nystagmus. Rev Neurol (Paris) 1970;124:526-530
8. Zifkin B, Andermann E, Andermann F, Kirkham T. An autosomal dominant syndrome of hemiplegic migraine, nystagmus, and tremor. Ann Neurol 1980;8:329-332
9. Joutel A, Bousser MG, Biousse V, et al. A gene for familial hemiplegic migraine maps to chromosome 19. Nat Genet 1993;5:40-45
10. Joutel A, Ducros A, Vahedi K, et al. Genetic heterogeneity of familial hemiplegic migraine. Am J Hum Genet 1994;55: 1166-1172
11. Ophoff RA, van Eijk R, Sandkuijl LA, et al. Genetic heterogeneity of familial hemiplegic migraine. Genomics 1994;22: 21-26
12. Elliott MA, Peroutka SJ, Welch S, May EF. Familial hemiplegic migraine, nystagmus, and cerebellar atrophy. Ann Neurol 1996;39:100-106
13. Ophoff RA, Terwindt GM, Vergouwe MN, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca(2+) channel gene CACNL1A4. Cell 1996;87:543-552
14. Gyapay G, Morissette J, Vignal A, et al. The 1993-94 Généthon human genetic linkage map. Nat Genet 1994;7:246-339
15. Lathrop GM, Lalouel JM. Easy calculation of lod scores and genetic risks on small computers. Am J Hum Genet 1984;36: 460-465
16. Ott J. Analysis of human genetic linkage. Baltimore: Johns Hopkins University Press, 1991
17. Ahmed MA, Reid E, Cooke A, et al. Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families. J Neurol Neurosurg Psychiatry 1996;61:616-620
18. Fletcher CF, Lutz CM, O'Sullivan TN, et al. Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Cell 1996;87:607-617
19. Diriong S, Lory P, Williams ME, et al. Chromosomal localization of the human genes for the alpha-1A, alpha 1-B, and alpha-1E voltage-dependent Ca(2+) channel subunits. Genomics 1995;30:605-609
20. Ptacek LJ, Tawil R, Griggs RC, et al. Dihydropyridine receptor mutations cause hypokalemic periodic paralysis. Cell 1994;77: 863-868
21. Schuler GD, Boguski MS, Stewart EA, et al. A gene map of the human genome. Science 1996;274:540-546
22. Lesage F, Fink M, Barhanin J, et al. Assignment of human G-protein-coupled inward rectifier K(+) channel homolog GIRK3 gene to chromosome 1q21-q23. Genomics 1995;29: 808-809
23. Lesage F, Duprat F, Fink M, et al. Cloning provides evidence for a family of inward rectifier and G-protein coupled K(+) channel in the brain. FEBS Lett 1994;353:37-42
24. Patil N, Cox DR, Bhat D, et al. A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation. Nat Genet 1995;11:126-129
25. Sakura H, Ammala C, Smith PA, et al. Characterization and variation of the human inwardly-rectifying K-channel (KCNJ6): a putative ATP-sensitive K-channel subunit. FEBS Lett 1995;336:193-196