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Severe hemophilia A due to a 1.3 kb factor VIII gene deletion including exon 24: homologous recombination between 41 bp within an Alu repeat sequence in introns 23 and 24

机译：严重的血友病A由于1.3 kB因子VIII基因缺失，包括外显子24：在内含子23和24中的ALU重复序列中的41bp之间的同源重组

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S. M. Nakaya; T.-C. Hsu; S. J. Geraghty; M. J. Manco-Johnson; A. R. Thompson;
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1. Severe hemophilia A due to a 1.3 kb factor VIII gene deletion including exon 24: homologous recombination between 41 bp within an Alu repeat sequence in introns 23 and 24. [J] . Nakaya SM, Hsu TC, Geraghty SJ, Journal of thrombosis and haemostasis: JTH . 2004,第11期

机译：由于1.3 kb因子VIII基因缺失（包括外显子24）而导致的严重血友病A：内含子23和24中Alu重复序列中41 bp之间的同源重组。
2. Severe haemophilia B due to a 6 kb factor IX gene deletion including exon 4: Non-homologous recombination associated with a shortened transcript from whole blood. [J] . Hsu TC, Nakaya SM, Thompson AR Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis . 2007,第2期

机译：由于6 kb因子IX基因缺失（包括外显子4）而导致的严重血友病B：与全血转录物缩短相关的非同源重组。
3. Non-homologous recombination between Alu and LINE-1 repeats results in a 91 kb deletion in MERTK causing severe retinitis pigmentosa [J] . Frida Jonsson, Marie Burstedt, Therese G. Kellgren, Molecular vision . 2018,第1期

机译：Alu和LINE-1重复序列之间的非同源重组导致MERTK缺失91 kb，从而导致严重的色素性视网膜炎
4. Non-homologous recombination between Alu and LINE-1 repeats results in a 91 kb deletion in MERTK causing severe retinitis pigmentosa [O] . Frida Jonsson, Marie Burstedt, Therese G. Kellgren, 2018

机译：Alu和LINE-1重复序列之间的非同源重组导致MERTK缺失91 kb从而导致严重的色素性视网膜炎
5. Non-homologous recombination between Alu and LINE-1 repeats caused a 430-kb deletion in the dystrophin gene: a novel source of genomic instability [O] . R. Suminaga, Y. Takeshima, K. Yasuda, 2000

机译：Alu和Line-1之间的非同源重组在肌营养蛋白基因中引起430kb缺失：基因组不稳定性的新来源

Severe hemophilia A due to a 1.3 kb factor VIII gene deletion including exon 24: homologous recombination between 41 bp within an Alu repeat sequence in introns 23 and 24

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