Screening and Analysis of Fibrillin-1 Gene ( FBN1) Mutation in a Chinese Family with Isolated Ectopia Lentis and Association Study of Schizophrenia and the Polymorphisms of COMT Gene in a Chinese Han Population 一个中国人单纯性晶状体异位家系FBN1基因突变的研究以及中国汉族精神分裂症与COMT基因多态性的关联性分析
Methods Clinical observation and pedigree analysis were undertaken in a family with ectopia lentis. 方法对单纯性晶状体异位一家系进行临床研究和系谱分析。
Novel mutation of fibrillin 1 gene cause ectopia lentis in a Chinese family 原纤维蛋白1基因新突变导致单纯性晶状体异位