Identification of F8 rearrangements in carrier and non‐carrier mothers of haemophilia A patients-Reference-Cited by-同舟云学术

Identification of F8 rearrangements in carrier and non‐carrier mothers of haemophilia A patients

Published:2021-08-11 Issue:5 Volume:27 Page:
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Manderstedt Eric¹^ORCID,Lind‐Halldén Christina¹,Ljung Rolf²^ORCID,Astermark Jan³^ORCID,Halldén Christer¹^ORCID

Affiliation:

1. Department of Environmental Science and Bioscience Kristianstad University Kristianstad Sweden

2. Department of Clinical Sciences – Paediatrics Lund University Lund Sweden

3. Department of Translational Medicine and Department of Haematology Oncology and Radiation Physics Centre for Thrombosis and Hemostasis Skåne University Hospital Malmö Sweden

Funder

Vetenskapsrådet

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.14394

Reference17 articles.

1. Genetic diagnosis in hemophilia and von Willebrand disease

2. Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A

3. Single-Tube Polymerase Chain Reaction for Rapid Diagnosis of the Inversion Hotspot of Mutation in Hemophilia A

4. Genotyping the Hemophilia Inversion Hotspot by Use of Inverse PCR

5. Developing a new generation of tests for genotyping hemophilia-causative rearrangements involvingint22handint1hhotspots in the factor VIII gene

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