Mutation analysis of Swedish haemophilia B families - high frequency of unique mutations.

Research output: Contribution to journalArticle

Abstract

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.

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Subject classification (UKÄ) – MANDATORY

  • Hematology
Original languageEnglish
JournalHaemophilia
Early online date2015 Nov 27
Publication statusPublished - 2015
Publication categoryResearch
Peer-reviewedYes