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

Mårtensson, Annika LU ; Letelier, A; Halldén, C and Ljung, Rolf LU (2015) In Haemophilia
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.
Please use this url to cite or link to this publication:
author
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Haemophilia
publisher
Federation of European Neuroscience Societies and Blackwell Publishing Ltd
external identifiers
  • pmid:26612714
  • scopus:84949908765
ISSN
1351-8216
DOI
10.1111/hae.12854
language
English
LU publication?
yes
id
abc4dc1a-18ed-4b2b-9b95-363ac353aca3 (old id 8234407)
alternative location
http://www.ncbi.nlm.nih.gov/pubmed/26612714?dopt=Abstract
date added to LUP
2015-12-02 19:54:44
date last changed
2017-07-30 04:47:54
@article{abc4dc1a-18ed-4b2b-9b95-363ac353aca3,
  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.},
  author       = {Mårtensson, Annika and Letelier, A and Halldén, C and Ljung, Rolf},
  issn         = {1351-8216},
  language     = {eng},
  month        = {11},
  publisher    = {Federation of European Neuroscience Societies and Blackwell Publishing Ltd},
  series       = {Haemophilia},
  title        = {Mutation analysis of Swedish haemophilia B families - high frequency of unique mutations.},
  url          = {http://dx.doi.org/10.1111/hae.12854},
  year         = {2015},
}