Mutation Profiling in Haemophilia A
Mutation Profiling in Haemophilia A
复制标题
血友病 A 的突变分析
DOI：
--
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发表时间：
2001
影响因子：
6.7
通讯作者：
J. Oldenburg
中科院分区：
文献类型：
--
作者：
J. Oldenburg
Summary Haemophilia A is a X-linked recessive bleeding disorder caused by deficiency or absence of coagulation factor VIII (FVIII) due to heterogeneous defects in the FVIII gene. The large size of the FVIII gene (26 exons spanning 186 kb) has hampered mutation analysis for many years. In 1991 the first systematic analysis of the complete coding region of the FVIII gene was performed by Higuchi et al. using Denaturing Gradient Gel Electrophoresis (DGGE) as a mutation screening method (1, 2). Notably, the causative mutation was not found in about half of the severely affected patients (1). This mystery was solved in 1993, when the intron 22 inversion was discovered (3, 4) that accounts for about 50% of the severe haemophilia A cases. The inversion mutation can be easily detected by Southern Blot. A recently described PCR-based method is more sophisticated, however once established, it allows rapid and convenient detection of the intron 22 inversion (5).
部分纠正了血友病 A 中因因子 VIII 基因表达过程中的错误而导致的严重分子缺陷。
影响因子：
9.8
作者：
Young,M;Inaba,H;Hoyer,LW;Higuchi,M;KazazianJr,HH;Antonarakis,SE
通讯作者：
Antonarakis,SE
DOI：
10.1073/pnas.88.16.7405
发表时间：
1991-08-01
影响因子：
11.1
作者：
HIGUCHI, M;KAZAZIAN, HH;ANTONARAKIS, SE
通讯作者：
ANTONARAKIS, SE