Savov A, Mercier B, Kalaydjieva L, Férec C
Laboratory of Molecular Pathology, University Obstetrics and Gynaecology Hospital, Sofia, Bulgaria.
Hum Mol Genet. 1994 Jan;3(1):57-60. doi: 10.1093/hmg/3.1.57.
The CFTR gene, in which more than 300 mutations have been described, displays a spectrum of mutations which varies according to ethnic and geographic origin of patients. In this paper we report an exhaustive study of the 27 exons and exon/intron boundaries of a sample of 35 CF patients from Bulgaria which is situated in the south east of Europe. We have used denaturing gradient gel electrophoresis assay followed by DNA sequencing and we report the identification of six previously undescribed CFTR alleles.
囊性纤维化跨膜传导调节因子(CFTR)基因已发现有300多种突变,其突变谱因患者的种族和地理来源而异。本文我们报告了对来自欧洲东南部保加利亚的35例囊性纤维化(CF)患者样本的27个外显子及外显子/内含子边界进行的详尽研究。我们采用了变性梯度凝胶电泳分析,随后进行DNA测序,并报告了六个先前未描述的CFTR等位基因的鉴定结果。