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

Neurology

Volumn 50, Issue 5, 1998, Pages 1428-1432

  Nyholt, D R ^a   Lea, R A ^a   Goadsby, P J ^b   Brimage, P J ^c   Griffiths, Lyn R ^a  

^a GRIFFITH UNIVERSITY   (Australia)

^b NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

^c PRINCE OF WALES HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 19; FAMILIAL DISEASE; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE SEGREGATION; GENETIC HETEROGENEITY; HUMAN; MIGRAINE; PRIORITY JOURNAL; TANDEM REPEAT;

EID: 0031844375     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.50.5.1428     Document Type: Article

References (35)

1. Kurtzke JF. The current neurologic burden of illness and injury in the United States. Neurology 1982;32:1207-1214.
2. Dalsgaard-Nielsen T, Ulrich J. Prevalence and heredity of migraine and migrainoid headaches among 461 Danish doctors. Headache 1972;12:168-172.
3. Stewart WF, Lipton RB, Celentano DD, Reed ML. Prevalence of migraine headache in the United States. JAMA 1992;267: 64-69.
4. Russell MB, Olesen J. The genetics of migraine without aura and migraine with aura. Cephalalgia 1992;13:245-248.
5. Mochi M, Sangiorgi S, Cortelli P, et al. Testing models for genetic determination in migraine. Cephalalgia 1993;13:389-394.
6. Blau JN. Migraine with and without aura are not different entities. Cephalalgia 1995;15:186-189.
7. Joutel A, Bousser M-G, Biousse V, et al. A gene for familial hemiplegic migraine maps to chromosome 19. Nat Genet 1993; 5:40-45.
8. Ophoff RA, Van Eijk R, Sandkuijl LA, et al. Genetic heterogeneity of familial hemiplegic migraine. Genomics 1994;22:21-26.
9. Ophoff RA, Terwindt GM, Vergouwe MN, et al. A 3 Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2; exclusion of PRKCSH as a candidate gene. Eur J Hum Genet 1996;4:321-328.
10. Joutel A, Ducros A, Vahedi K, et al. Genetic heterogeneity of familial hemiplegic. Am J Hum Genet 1994;55:1166-1172.
11. 2+ channel gene CACNL1A4. Cell 1996;87: 543-552.
12. Hovatta L, Kallela M, Farkkila M, Peltonen L. Familial migraine: exclusion of the susceptibility gene from the reported locus of familial hemiplegic migraine on 19p. Genomics 1994; 23:707-709.
13. May A, Ophoff RA, Terwindt GM, et al. Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura. Hum Genet 1995;96:604-608.
14. 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.
15. Griffiths LR, Nyholt DR, Curtain RP, Goadsby PJ, Brimage PJ. Migraine association and linkage studies of an endothelial nitric oxide synthase (NOS3) gene polymorphism. Neurology 1997;49:614-617.
16. Blin N, Stafford DW. Isolation of high molecular-weight DNA. Nucleic Acids Res 1976;3:2303.
17. Miller SA, Dykes DD, Plensky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988;16:1215.
18. Gyapay G, Morissette J, Vignal A, et al. The 1993-94 Genethon human genetic linkage map. Nat Genet 1994;7:246-339.
19. Johns Hopkins University School of Medicine, host. The genome database. Baltimore (http://gdbwww.gdb.org/gdb/ gdbtop.html/).
20. Boehnke M. Allele frequency estimation from data on relatives. Am J Hum Genet 1991;48:22-25.
21. Lathrop GM, Lalouel JM, Julier C, Ott J. Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Hum Genet 1985;37:482-498.
22. Cottingham RW Jr, Idury RM, Schaffer AA. Faster sequential genetic linkage computations. Am J Hum Genet 1993;53:252-263.
23. Schaffer AA, Gupta SK, Shiram K, Cottingham RW Jr. Avoiding recomputation in linkage analysis. Hum Hered 1994;44: 225-237.
24. O'Connell JR, Weeks DE. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nat Genet 1995;11:402-408.
25. Curtis D, Gurling HMD. A procedure for combining two-point lod scores into a summary multipoint map. Hum Hered 1993; 43:173-185.
26. Ott J. Analysis of human genetic linkage. Baltimore: Johns Hopkins University Press, 1991.
27. Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. Parametric and non-parametric linkage analysis: a unified multipoint approach. Am J Hum Genet 1996;58:1347-1363.
28. Risch N. Linkage strategies of genetically complex traits. I. Multilocus models. Am J Hum Genet 1990;46:222-228.
29. Terwilliger JD, Ott J. Handbook of genetic linkage. Baltimore: Johns Hopkins University Press, 1994.
30. Zhuchenko O, Bailey J, Bonnen P, et al. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha(1A)-voltage-dependent calcium channel. Nat Genet 1997;15:62-69.
31. 2+ channel subunits. Genomics 1995;30:605-609.
32. 2+ channel (CACNL1A3) to chromosome 1q31-32. Genomics 1993;15:107-112.
33. Iles DE, Segers B, Weghuis DO, et al. Refined localisation of the alpha-1 subunit of the skeletal muscle L-type voltage dependent calcium channel (CACNL1A3) to human chromosome 1q32 by in situ hybridization. Genomics 1994;19:561-563.
34. Litt M, Kramer P, Browne DL, et al. A gene for episodic ataxia/myokymia maps to chromosome 12p13. Am J Hum Genet 1994;55:702-709.
35. Browne DL, Gancer ST, Nutt JG, et al. Episodic ataxia/ myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1. Nat Genet 1994;8: 136-140.