No evidence for linkage between schizophrenia and eight microsatellite markers on chromosome 19

被引:6
|
作者
Parfitt, E
Asherson, P
Roberts, E
Mant, R
Nanko, S
Gill, M
McGuffin, P
Owen, M
机构
[1] UNIV WALES COLL CARDIFF,COLL MED,DEPT PSYCHOL MED,CARDIFF CF4 4XN,S GLAM,WALES
[2] UNIV WALES COLL CARDIFF,COLL MED,DEPT MED GENET,CARDIFF CF4 4XN,S GLAM,WALES
[3] INST PSYCHIAT,LONDON,ENGLAND
[4] TEIKYO UNIV,SCH MED,TOKYO 173,JAPAN
[5] TRINITY CTR HLTH SCI,DEPT PSYCHIAT,DUBLIN,IRELAND
基金
英国惠康基金; 英国医学研究理事会;
关键词
schizophrenia; linkage analysis; chromosome; 19;
D O I
10.1159/000154352
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report the results of a linkage study of eight markers on chromosome 19 in a sample of 24 families multiply affected with schizophrenia and related psychoses, This study forms part of a systematic search of the entire genome using microsatellite markers spaced at 10-20 cM intervals. These data provide no evidence for the presence of a gene of major effect on chromosome 19 under the assumption of genetic homogeneity or heterogeneity, We have attempted to describe the extent to which this region has been excluded and demonstrate that while it is possible to exclude near-dominant and recessive models under the assumption that all families are linked Schizophrenia to the same locus, power for exclusion falls away rapidly when Linkage analysis incomplete penetrance and heterogeneity are invoked.
引用
收藏
页码:191 / 196
页数:6
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