Tsui L C
Department of Genetics, Hospital for Sick Children, Toronto, Ontario, Canada.
Trends Genet. 1992 Nov;8(11):392-8. doi: 10.1016/0168-9525(92)90301-j.
Although the major mutation causing cystic fibrosis accounts for almost 70% of mutant chromosomes screened, almost 300 sequence alterations have been identified in the gene during the past two and a half years. At least 230 of these mutations are probably associated with disease. This rapid accumulation of data is in part due to the highly coordinated effort by members of the Cystic Fibrosis Genetic Analysis Consortium. The information is not only essential to genetic diagnosis, but also will aid in understanding the structure and function of the protein, and possibly in correlating genotype with phenotype.
尽管导致囊性纤维化的主要突变在筛查的突变染色体中占近70%,但在过去两年半的时间里,该基因已鉴定出近300种序列改变。其中至少230种突变可能与疾病相关。数据的快速积累部分归功于囊性纤维化基因分析联盟成员的高度协作努力。这些信息不仅对基因诊断至关重要,还将有助于理解该蛋白质的结构和功能,并可能有助于将基因型与表型相关联。