Reiss J, Lenz U, Rininsland F, Ballhausen P, Drews D, Posselt H G
Institut für Humangenetik der Universität, Göttingen, Federal Republic of Germany.
Hum Genet. 1992 Nov;90(3):303-4. doi: 10.1007/BF00220085.
German cystic fibrosis patients were screened for mutations in exon 21 of the cystic fibrosis transmembrane conductance regulator gene by a non-radioactive variation of the single-strand conformation polymorphism technique. Asymmetric polymerase chain reaction amplification was used to produce single strands of exon-containing genomic sequences that were analyzed on polyacrylamide gels subsequently stained with ethidium bromide. This rapid technique led to the identification of a novel mutation, a 1-bp deletion at position 4035(A) of the cDNA sequence. The patient, who is also heterozygous for the delta F508 mutation, exhibits an intermediate form of the disease.
通过单链构象多态性技术的非放射性变体,对德国囊性纤维化患者进行囊性纤维化跨膜传导调节基因第21外显子突变的筛查。采用不对称聚合酶链反应扩增来产生含外显子的基因组序列单链,这些单链在随后用溴化乙锭染色的聚丙烯酰胺凝胶上进行分析。这种快速技术导致鉴定出一种新的突变,即cDNA序列第4035位(A)处1个碱基对的缺失。该患者同时也是ΔF508突变的杂合子,表现出疾病的中间形式。