Profiling of F8 gene mutations in 262 Chinese haemophilia A patients

被引：0
|
作者：
Lu, Y. [1 ]
Wang, X. [1 ]
Ding, Q. [1 ]
Dai, J. [1 ]
Wang, H. [2 ]
Xi, X.
机构：
[1] Jiao Tong Univ, Coll Med, Ruijin Hosp, Clin Transfus Dept, Chengdu, Peoples R China
[2] Shanghai Inst Hematol, Shanghai, Peoples R China
来源：
JOURNAL OF THROMBOSIS AND HAEMOSTASIS | 2011年 / 9卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：211 / 211
页数：1
相关论文
共 50 条
  • [21] F8 gene mutation profile and immune tolerance induction outcome in patients with severe haemophilia A with inhibitors
    Rossetti, Liliana
    Ziegler, Betiana
    Marchione, Vanina
    Radic, Pamela
    Abelleyro, Martin
    Neme, Daniela
    Cocca, Andrea
    De Brasi, Carlos
    HAEMOPHILIA, 2023, 29 : 6 - 6
  • [22] A recurrent F8 mutation in Irish haemophilia A patients:: evidence for a founder effect
    Winter, P. C.
    Egan, H.
    Mcnulty, O.
    Jones, F. G. C.
    O'Donnell, J.
    Jenkins, P. V.
    HAEMOPHILIA, 2008, 14 (02) : 394 - 395
  • [23] F8 locus itself seems to explain all cases of hemophilia a patients without mutations in the F8 cDNA
    El-Maarri, O.
    Pezeshkpoor, B.
    Vidocich, N.
    Nuesgen, N.
    Nanda, I
    Haaf, T.
    Budde, U.
    Oldenburg, J.
    El-Maarri, O.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 : 212 - 212
  • [24] Mutation analysis in the F8 gene in 485 families with haemophilia A and prenatal diagnosis in China
    Feng, Yin
    Li, Qianqian
    Shi, Panlai
    Liu, Ning
    Kong, Xiangdong
    Guo, Ruixia
    HAEMOPHILIA, 2021, 27 (01) : E88 - E92
  • [25] Identification of Novel Mutations in Exon 14 of the F8 Gene in Malaysian Patients with Severe Hemophilia A
    Emmanuel Jairaj Moses
    Sim Pei Ling
    Faisal Muti Al-Hassan
    Faraizah Abdul Karim
    Narazah Mohd Yusoff
    Indian Journal of Clinical Biochemistry, 2012, 27 (2) : 207 - 208
  • [26] Influence of the type of F8 gene mutation on inhibitor development in a single centre cohort of severe haemophilia A patients
    Gouw, S. C.
    Van der Bom, J. G.
    Van den Berg, H. M.
    Zewald, R. A.
    Van Amstel, J. K. Ploos
    Mauser-Bunschoten, E. P.
    HAEMOPHILIA, 2011, 17 (02) : 275 - 281
  • [27] Mutation spectrum of F8 gene in Turkish hemophilia A patients: identification of 14 novel mutations
    Atik, T.
    Isik, E.
    Akgun, B.
    Onay, H.
    Kavakli, K.
    Ozbek, N. Y.
    Evim, M.
    Balkan, C.
    Gunes, A. M.
    Culha, V.
    Unal, E.
    Belen, F. B.
    Sahin, F.
    Ozkinay, F.
    HAEMOPHILIA, 2018, 24 : 128 - 128
  • [28] SVA RETROTRANSPOSON INSERTION IN EXON 14 OF F8 GENE CAUSES SEVERE HAEMOPHILIA A
    Pshenichnikova, O.
    Salomashkina, V.
    Perina, F.
    Surin, V.
    HAEMOPHILIA, 2023, 29 : 33 - 33
  • [29] Identification of Novel Mutations in Exon 14 of the F8 Gene in Malaysian Patients with Severe Hemophilia A
    Moses, Emmanuel Jairaj
    Ling, Sim Pei
    Al-Hassan, Faisal Muti
    Karim, Faraizah Abdul
    Yusoff, Narazah Mohd
    INDIAN JOURNAL OF CLINICAL BIOCHEMISTRY, 2012, 27 (02) : 207 - 208
  • [30] Identification of F8 rearrangements in carrier and non-carrier mothers of haemophilia A patients
    Manderstedt, Eric
    Lind-Hallden, Christina
    Ljung, Rolf
    Astermark, Jan
    Hallden, Christer
    HAEMOPHILIA, 2021, 27 (05) : E654 - E658
12345