Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32

被引:91
作者
Lin, MW
Curtis, D
Williams, N
Arranz, M
Nanko, S
Collier, D
McGuffin, P
Murray, R
Owen, M
Gill, M
Powell, J
机构
[1] INST PSYCHIAT,DEPT NEUROSCI,LONDON SE5 8AF,ENGLAND
[2] INST PSYCHIAT,DEPT PSYCHOL MED,LONDON SE5 8AF,ENGLAND
[3] UNIV WALES COLL MED,DEPT PSYCHOL MED,CARDIFF CF4 4XN,S GLAM,WALES
[4] TEIKYO UNIV,SCH MED,DEPT PSYCHIAT,TOKYO 173,JAPAN
[5] ST JAMES HOSP,TRINITY CTR HLTH SCI,DEPT PSYCHIAT,DUBLIN,IRELAND
关键词
chromosome; 13; heterogeneity; linkage analysis; schizophrenia;
D O I
10.1097/00041444-199505030-00004
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Family, twin and adoption studies highlight the influence of genes in the aetiology of schizophrenia, though the mode of inheritance is unclear. We have been conducting a systematic search for major genes in schizophrenia using a series of multiply affected families and report preliminary results of linkage under heterogeneity with markers on chromosome 13, A lod2 score of 1.61 for marker D13S144 was obtained at theta = 0 and alpha of 0.5 and nearby markers also produced positive values.
引用
收藏
页码:117 / 126
页数:10
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