Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

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

Mårtensson, Annika LU ; Letelier, A ; Halldén, C and Ljung, Rolf LU orcid (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
; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Haemophilia
publisher
Wiley-Blackwell
external identifiers
  • pmid:26612714
  • scopus:84949908765
  • pmid:26612714
  • wos:000379715000042
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
2016-04-04 07:18:12
date last changed
2022-08-08 05:55:22
@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    = {{Wiley-Blackwell}},
  series       = {{Haemophilia}},
  title        = {{Mutation analysis of Swedish haemophilia B families - high frequency of unique mutations.}},
  url          = {{http://dx.doi.org/10.1111/hae.12854}},
  doi          = {{10.1111/hae.12854}},
  year         = {{2015}},
}