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:
https://lup.lub.lu.se/record/8234407
- author
- Mårtensson, Annika
LU
; Letelier, A
; Halldén, C
and Ljung, Rolf
LU
- organization
- publishing date
- 2015-11-27
- 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}},
}