Genetic analysis of bleeding disorders-Reference-Cited by-同舟云学术

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Genetic analysis of bleeding disorders

Published:2016-07 Issue: Volume:22 Page:79-83
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Edison E.¹,Konkle B. A.²,Goodeve A. C.³⁴

Affiliation:

1. Department of Haematology; Christian Medical College; Vellore India

2. Bloodworks Northwest and University of Washington; Seattle WA USA

3. Sheffield Diagnostic Genetics Service; Sheffield Children's NHS Foundation Trust; Sheffield UK

4. Department of Infection, Immunity and Cardiovascular Disease; University of Sheffield; Sheffield UK

Funder

Biogen

CSL Behring

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Reference14 articles.

1. Informativeness of linkage analysis for genetic diagnosis of haemophilia A in India;Jayandharan;Haemophilia,2004

2. Genotyping the hemophilia inversion hotspot by use of inverse PCR;Rossetti;Clin Chem,2005

3. Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A;Bagnall;Blood,2002

4. Precise carrier diagnosis in families with haemophilia A: use of conformation sensitive gel electrophoresis for mutation screening and polymorphism analysis;Williams;Thromb Haemost,1998

5. Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin;Jayandharan;J Thromb Haemost,2005

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Challenges and opportunities when transitioning from in vivo gene replacement to in vivo CRISPR/Cas9 therapies – a spotlight on hemophilia;Expert Opinion on Biological Therapy;2022-06-21

2. Hemophilia A gene therapy: current and next-generation approaches;Expert Opinion on Biological Therapy;2022-01-06

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