UK Haemophilia Centre Doctors' Organization Haemophilia Genetics Laboratory Network
The molecular analysis of haemophilia A: a guideline from the UK haemophilia centre doctors' organization haemophilia genetics laboratory network
Abstract
Haemophilia A is a common inherited bleeding disorder that has a well-understood pathophysiology. Our understanding of the molecular genetics of the disease has allowed the development of comprehensive carrier and prenatal diagnosis for this single gene defect. Continuing technological developments improve our ability to provide genetic analysis in a rapid and cost effective manner. This guideline aims to provide advice on current best laboratory practice when approaching genetic diagnosis of haemophilia A.
Source and rights
Published by Haemophilia : the official journal of the World Federation of Hemophilia, 2005. The guideline itself is at the source linked here.
Prognia summarises this guideline for reference and education. It is not medical advice. Always check the official guideline and current local protocols before acting on it.
At a glance
- Organisation
- UK Haemophilia Centre Doctors' Organization Haemophilia Genetics Laboratory Network
- Published
- 2005
- Applies to
- 🇬🇧 United Kingdom
- Scope
- National
- Journal
- Haemophilia : the official journal of the World Federation of Hemophilia
- PubMed
- 16011593
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