Ginns E I, Egeland J A, Allen C R, Pauls D L, Falls K, Keith T P, Paul S M
Section on Molecular Neurogenetics, NIMH, Bethesda, MD 20892.
J Psychiatr Res. 1992 Oct;26(4):305-8. doi: 10.1016/0022-3956(92)90037-o.
In this report we describe our efforts to identify a gene involved in bipolar illness using a large, multigenerational Old Order Amish pedigree with many affected individuals. The original collection of cell lines from Amish pedigree 110 has been extended to include 169 individuals. We have used over 250 markers spaced at approximately 20 centiMorgans that detect restriction length fragment polymorphisms, but no LOD scores greater than 3 have been obtained from pairwise linkage analyses. We are expanding our collection of cell lines from both normal and affected family members and updating our diagnostic data as we continue our systematic screening of the genome for a gene involved in bipolar illness.
在本报告中,我们描述了我们利用一个有许多患病个体的大型多代旧秩序阿米什人谱系来鉴定一个与双相情感障碍相关基因的工作。来自阿米什人谱系110的原始细胞系已扩展至包括169名个体。我们使用了约250个间隔约20厘摩的标记,这些标记可检测限制性片段长度多态性,但从成对连锁分析中未获得大于3的对数优势分数。随着我们继续对基因组进行系统筛查以寻找与双相情感障碍相关的基因,我们正在扩大正常和患病家庭成员的细胞系收集,并更新我们的诊断数据。