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C1抑制因子基因核苷酸插入导致II型遗传性血管性水肿。

C1-inhibitor gene nucleotide insertion causes type II hereditary angio-oedema.

作者信息

Siddique Z, McPhaden A R, Whaley K

机构信息

University Department of Pathology, Western Infirmary, Glasgow.

出版信息

Hum Genet. 1993 Sep;92(2):189-90. doi: 10.1007/BF00219690.

Abstract

The polymerase chain reaction and nucleotide sequence analysis have been used to characterise a three nucleotide insertion in the eighth exon of one allele of the C1-inhibitor gene between nucleotides 16749 and 16750 in a kindred with type II hereditary angio-oedema (HAE). The effect of the resulting C1-inhibitor amino acid sequence alteration is discussed. This represents the first report of a nucleotide insertion in the C1-inhibitor gene causing type II HAE.

摘要

聚合酶链反应和核苷酸序列分析已被用于鉴定Ⅱ型遗传性血管性水肿(HAE)家系中C1抑制因子基因一个等位基因第八外显子中16749和16750位核苷酸之间的三核苷酸插入。文中讨论了由此导致的C1抑制因子氨基酸序列改变的影响。这是关于C1抑制因子基因中导致Ⅱ型HAE的核苷酸插入的首次报道。

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