Shaikh S, Gill M, Owen M, Asherson P, McGuffin P, Nanko S, Murray R M, Collier D A
Department of Neuropathology, Institute of Psychiatry, London, England.
Am J Med Genet. 1994 Mar 15;54(1):8-11. doi: 10.1002/ajmg.1320540104.
We report the results of a linkage study in 24 families multiply affected with schizophrenia using a polymorphic DNA sequence encoding the third cytoplasmic loop of the dopamine D4 receptor. Two-point LOD score analyses with a range of single gene models ranging from near dominant to near recessive revealed no evidence for linkage. In addition, we examined the data by non-parametric sib-pair analysis and found no excess sharing of alleles between affected sib-pairs. We therefore conclude that mutations within the dopamine D4 receptor gene do not have a major aetiological role in schizophrenia in our collection of pedigrees.
我们报告了一项连锁研究的结果,该研究使用编码多巴胺D4受体第三细胞质环的多态性DNA序列,对24个精神分裂症多发家系进行了研究。采用一系列从近显性到近隐性的单基因模型进行两点LOD评分分析,未发现连锁证据。此外,我们通过非参数同胞对分析检查了数据,发现患病同胞对之间没有等位基因的过度共享。因此,我们得出结论,在我们收集的家系中,多巴胺D4受体基因内的突变在精神分裂症中不具有主要病因学作用。