Mutation analysis of Swedish haemophilia B families - high frequency of unique mutations.
Research output: Contribution to journal › Article
Haemophilia B is caused by a heterogeneous spectrum of mutations. Mutation characterization is important in genetic counselling, prenatal diagnosis and to predict risk of inhibitor development.
|Research areas and keywords||
Subject classification (UKÄ) – MANDATORY
|Early online date||2015 Nov 27|
|Publication status||Published - 2015|