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Chapter 1 Profiling of Mutations in the F8 and F9, Causative Genes of Hemophilia A and Hemophilia B'

机译：第1章F8和F9中的突变分析，血友病A和血友病的致病基因

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Sung Ho; Hee-Jin Kim; Hye Sun;
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1. Screening of mutations of hemophilia A in 40 Italian patients: a novel G-to-A mutation in intron 10 of the F8 gene as a putative cause of mild hemophilia A in southern Italy. [J] . Santacroce R, Santoro R, Sessa F, Blood coagulation & fibrinolysis: an international journal in haemostasis and thrombosis . 2008,第3期

机译：40名意大利患者血友病A突变的筛查：F8基因内含子10中新的G-to-A突变是意大利南部轻度血友病A的推定原因。
2. F8 gene mutation profile in Indian hemophilia A patients: Identification of 23 novel mutations and factor VIII inhibitor risk association [J] . Patricia Pinto, Kanjaksha Ghosh, Shrimati Shetty Mutation research-Fundamental and Molecular Mechanisms of Mutagenesis . 2016,第Null期

机译：印度血友病A患者的F8基因突变概况：鉴定23种新突变与因子VIII抑制剂的风险关联
3. Clinical manifestation of hemophilia A in the absence of mutations in the F8 F8 gene that encodes FVIII: role of microRNAs [J] . Jankowska Katarzyna I., McGill Joseph, Pezeshkpoor Behnaz, Transfusion: The Journal of the American Association of Blood Banks . 2020,第2期

机译：编码FVIII的F8 F8基因突变中血友病A中血友病A的临床表现：MicroRNA的作用
4. Investigation of Underlying Reasons of Factor VIM Deficiency in Hemophilia A Patients with Undetectable Mutations in the F8 Gene [C] . O.El-Maarri, C.Klein, J.Schroder, Hemophilia Symposium . 2008

机译：血友病因子vim缺乏症患者F8基因患者
5. Gene therapy for hemophilia A: Targeting long-term hematopoietic repopulating cells with a retroviral vector expressing a bioengineered human factor VIII gene [D] . Moayeri, Morvarid 2005

机译：血友病A的基因治疗：用表达生物工程化人类因子VIII基因的逆转录病毒载体靶向长期造血的繁殖细胞
6. Hemophilia A: different phenotypes may be explained by multiple and variable effects of the causative mutation in the F8 gene [O] . Giancarlo Castaman 2018

机译：血友病A：不同的表型可能是由F8基因致病性突变的多重和可变影响所解释的
7. Hemophilia A: different phenotypes may be explained by multiple and variable effects of the causative mutation in the F8 gene [O] . Giancarlo Castaman 2018

机译：血友病A：不同的表型可以通过F8基因中的致病性突变的多种和可变效应来解释

﻿Chapter 1 Profiling of Mutations in the F8 and F9, Causative Genes of Hemophilia A and Hemophilia B'

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Chapter 1 Profiling of Mutations in the F8 and F9, Causative Genes of Hemophilia A and Hemophilia B'