The missense mutation in the WKL1 gene not found in patients with bipolar affective disorder

被引:4
作者
Ewald, H [1 ]
Lundorf, MD
机构
[1] Hosp Psychiat, Inst Basic Psychiat Res, Dept Biol Psychiat, DK-8240 Risskov, Denmark
[2] Hosp Psychiat, Dept Psychiat Demog, DK-8240 Risskov, Denmark
关键词
D O I
10.1038/sj.mp.4001002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
引用
收藏
页码:340 / 341
页数:2
相关论文
共 9 条
[1]   Two novel variants in the DOPA decarboxylase gene: association with bipolar affective disorder [J].
Borglum, AD ;
Bruun, TG ;
Kjeldsen, TE ;
Ewald, H ;
Mors, O ;
Kirov, G ;
Russ, C ;
Freeman, B ;
Collier, DA ;
Kruse, TA .
MOLECULAR PSYCHIATRY, 1999, 4 (06) :545-551
[2]  
Bruun TG, 1999, MOL PSYCHIATR, V4, P414
[3]   Characterization of single-nucleotide polymorphisms in coding regions of human genes [J].
Cargill, M ;
Altshuler, D ;
Ireland, J ;
Sklar, P ;
Ardlie, K ;
Patil, N ;
Lane, CR ;
Lim, EP ;
Kalyanaraman, N ;
Nemesh, J ;
Ziaugra, L ;
Friedland, L ;
Rolfe, A ;
Warrington, J ;
Lipshutz, R ;
Daley, GQ ;
Lander, ES .
NATURE GENETICS, 1999, 22 (03) :231-238
[4]   GENETIC DISSECTION OF COMPLEX TRAITS - GUIDELINES FOR INTERPRETING AND REPORTING LINKAGE RESULTS [J].
LANDER, E ;
KRUGLYAK, L .
NATURE GENETICS, 1995, 11 (03) :241-247
[5]   Initial sequencing and analysis of the human genome [J].
Lander, ES ;
Int Human Genome Sequencing Consortium ;
Linton, LM ;
Birren, B ;
Nusbaum, C ;
Zody, MC ;
Baldwin, J ;
Devon, K ;
Dewar, K ;
Doyle, M ;
FitzHugh, W ;
Funke, R ;
Gage, D ;
Harris, K ;
Heaford, A ;
Howland, J ;
Kann, L ;
Lehoczky, J ;
LeVine, R ;
McEwan, P ;
McKernan, K ;
Meldrim, J ;
Mesirov, JP ;
Miranda, C ;
Morris, W ;
Naylor, J ;
Raymond, C ;
Rosetti, M ;
Santos, R ;
Sheridan, A ;
Sougnez, C ;
Stange-Thomann, N ;
Stojanovic, N ;
Subramanian, A ;
Wyman, D ;
Rogers, J ;
Sulston, J ;
Ainscough, R ;
Beck, S ;
Bentley, D ;
Burton, J ;
Clee, C ;
Carter, N ;
Coulson, A ;
Deadman, R ;
Deloukas, P ;
Dunham, A ;
Dunham, I ;
Durbin, R ;
French, L .
NATURE, 2001, 409 (6822) :860-921
[6]   A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree [J].
Meyer, J ;
Huberth, A ;
Ortega, G ;
Syagailo, YV ;
Jatzke, S ;
Mössner, R ;
Strom, TM ;
Ulzheimer-Teuber, I ;
Stöber, G ;
Schmitt, A ;
Lesch, KP .
MOLECULAR PSYCHIATRY, 2001, 6 (03) :302-306
[7]   Splitting schizophrenia:: Periodic catatonia-susceptibility locus on chromosome 15q15 [J].
Stöber, G ;
Saar, K ;
Rüschendorf, F ;
Meyer, J ;
Nürnberg, G ;
Jatzke, S ;
Franzek, E ;
Reis, A ;
Lesch, KP ;
Wienker, TF ;
Beckmann, H .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (05) :1201-1207
[8]  
VOGEL F, 1996, HUMAN GENETICS PROBL
[9]  
*WHO, 1996, SCHED CLIN ASS NEUR