Polymorphisms of casein kinase I gamma 2 gene associated with simple febrile seizures in Chinese Han population

Neuroscience Letters

Volumn 368, Issue 1, 2004, Pages 2-6

  Yinan, Ma ^a   Yu, Qi ^a   Zhiyue, Chen ^a   Jianjun, Lu ^a   Lie, Hao ^a   Liping, Zou ^b   Jianhui, Zhang ^c   Fang, Sun ^a   Dingfang, Bu ^a   Qing, Lin ^a   Xiru, Wu ^a  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

^b CAPITAL MEDICAL UNIVERSITY   (China)

^c Hebei Cancer Institute   (China)

Author keywords

Chinese; CSNK1G2 gene; Haplotype; Simple febrile seizures; Single nucleotide polymorphisms

Indexed keywords

CASEIN KINASE I;

ADOLESCENT; ARTICLE; BRAIN DEVELOPMENT; CONTROLLED STUDY; DATA ANALYSIS; DNA FLANKING REGION; FEBRILE CONVULSION; FEMALE; GENE AMPLIFICATION; GENE FUNCTION; GENE SEQUENCE; GENETIC LINKAGE; GENETIC POLYMORPHISM; HUMAN; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SYNAPSE VESICLE;

ALLELES; CASEIN KINASE I; CHINA; ETHNIC GROUPS; EXONS; FEVER; GENE FREQUENCY; GENETIC MARKERS; HAPLOTYPES; HUMANS; INTRONS; LINKAGE (GENETICS); POLYMORPHISM, SINGLE NUCLEOTIDE; SEIZURES;

EID: 4444361243     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2004.06.054     Document Type: Article

References (19)

1. S.E. Antonarakis Nomenclature Working Group Recommendations for a nomenclature system for human gene mutations Hum. Mutat. 11 1998 1 3
2. I.C. Chou, C.T. Peng, F.J. Tsai, C.C. Huang, Y.R. Shi, and C.H. Tsai The lack of association between febrile convulsions and polymorphisms in SCN1A Epilepsy Res. 54 2003 53 57
3. S.D. Gross, and R.A. Anderson Casein kinase I: spatial organization and positioning of a multifunctional protein kinase family Cell Signal. 10 1998 699 711
4. S. Hirose, R.P. Mohney, M. Okada, S. Kaneko, and A. Mitsudome The genetics of febrile seizures and related epilepsy syndromes Brain Dev. 25 2003 304 312
5. E.W. Johnson, J. Dubovsky, S.S. Rich, C.A. O'Donovan, H.T. Orr, V.E. Anderson, A. Gil-Nagel, P. Ahmann, C.G. Dokken, D.T. Schneider, and J.L. Weber Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest Hum. Mol. Genet. 7 1998 63 67
6. A.N. Kitabayashi, J. Kusuda, M. Hirai, and K. Hashimoto Cloning and chromosomal mapping of human casein kinase 1 γ2 (CSNK1G2) Genomics 46 1997 133 137
7. S.L. Kugler, E.S. Stenroos, D.E. Mandelbaum, T. Lehner, V.V. McKoy, T. Prossick, J. Sasvari, K. Swannick, J. Katz, and W.G. Johnson Hereditary febrile seizures: phenotype and evidence for a chromosome 19p locus Am. J. Med. Genet. 79 1998 354 361
8. F. Liu, D.M. Virshup, A.C. Nairn, and P. Greengard Mechanism of regulation of casein kinase I activity by group I metabotropic glutamate receptors J. Biol. Chem. 277 2002 45393 45399
9. S.A. Miller, D.D. Dyhes, and H.F. Poleskey A simple salting out procedure for extracting DNA from human nucleated cells Nucleic Acids Res. 16 1988 1215
10. R. Nabbout, J.F. Prud'homme, A. Herman, J. Feingold, A. Brice, O. Dulac, and E. Leguern A locus for simple pure febrile seizures maps to chromosome 6q22-q24 Brain 125 2002 2668 2680
11. J. Nakayama, Y.H. Fu, A.M. Clark, S. Nakahara, K. Hamano, N. Iwasaki, A. Matsui, T. Arinami, and L.J. Ptacek A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures Ann. Neurol. 52 2002 654 657
12. J. Nakayama, K. Hamano, N. Iwasaki, S. Nakahara, Y. Horigome, H. Saitoh, T. Aoki, T. Maki, M. Kikuchi, T. Migita, T. Ohto, Y. Yokouchi, R. Tanaka, M. Hasegawa, A. Matsui, H. Hamaguchi, and T. Arinami Significant evidence for linkage of febrile seizures to chromosome 5q14-q15 Hum. Mol. Genet. 9 2000 87 91
13. J. Nakayama, K. Hamano, E. Noguchi, Y. Horiuchi, N. Iwasaki, M. Ohta, S. Nakahara, T. Naoi, A. Matsui, and T. Arinami Failure to find causal mutations in the GABAA-receptor γ2 subunit (GABRG2) gene in Japanese febrile seizure patients Neurosci. Lett. 343 2003 117 120
14. J. Nakayama, N. Yamamoto, K. Hamano, N. Iwasaki, M. Ohta, S. Nakahara, Y. Horigome, C. Nakahara, E. Noguchi, J. Shiono, Y. Shimakura, K. Yamakawa-Kobayashi, A. Matsui, and T. Arinami Failure to find evidence for association between voltage-gated sodium channel gene SCN2A variants and febrile seizures in humans Neurosci. Lett. 329 2002 249 251
15. A. Peiffer, J. Thompson, C. Charlier, B. Otterud, T. Varvil, C. Pappas, C. Barnitz, K. Gruenthal, R. Kuhn, and M. Leppert A locus for febrile seizures (FEB3) maps to chromosome 2q23-24 Ann. Neurol. 46 1999 671 678
16. Y. Qi, J.J. Lv, X.R. Wu, X.H. Pan, H. Bao, J. Peng, and Q. Lin Familial febrile convulsions is supposed to link to human chromosome 19p13.3 Zhonghua Yi Xue Za Zhi. 81 2001 27 29
17. M.D. Shriver, E.J. Parra, S. Dios, C. Bonilla, H. Norton, C. Jovel, C. Pfaff, C. Jones, A. Massac, N. Cameron, A. Baron, T. Jackson, G. Argyropoulos, L. Jin, C.J. Hoggart, P.M. McKeigue, and R.A. Kittles Skin pigmentation, biogeographical ancestry and admixture mapping Hum. Genet. 112 2003 387 399
18. H.K. Tabor, N.J. Risch, and R.M. Myers Candidate-gene approaches for studying complex genetic traits: practical considerations Nat. Rev. Genet. 3 2002 391 397
19. R.H. Wallace, S.F. Berkovic, R.A. Howell, G.R. Sutherland, and J.C. Mulley Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21 J. Med. Genet. 33 1996 308 312