FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon
(2018) In Blood Transfusion 16. p.101-104
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/d1529808-bad1-46d7-a302-32d047b76528
- author
- Michalewska, Bogumila
; Olsson, Martin L
LU
; Naremska, Grazyna
; Walenciak, Jolanta
; Hult, Annika K
LU
; Ozog, Agnieszka
; Guz, Katarzyna
; Brojer, Ewa
and Storry, Jill R
LU
- organization
- publishing date
- 2018-01
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Blood Transfusion
- volume
- 16
- pages
- 101 - 104
- publisher
- Edizioni SIMTI
- external identifiers
-
- pmid:27893357
- scopus:85041193197
- ISSN
- 1723-2007
- DOI
- 10.2450/2016.0135-16
- language
- English
- LU publication?
- yes
- id
- d1529808-bad1-46d7-a302-32d047b76528
- date added to LUP
- 2017-04-29 19:00:31
- date last changed
- 2025-10-14 23:41:04
@article{d1529808-bad1-46d7-a302-32d047b76528,
author = {{Michalewska, Bogumila and Olsson, Martin L and Naremska, Grazyna and Walenciak, Jolanta and Hult, Annika K and Ozog, Agnieszka and Guz, Katarzyna and Brojer, Ewa and Storry, Jill R}},
issn = {{1723-2007}},
language = {{eng}},
pages = {{101--104}},
publisher = {{Edizioni SIMTI}},
series = {{Blood Transfusion}},
title = {{FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon}},
url = {{http://dx.doi.org/10.2450/2016.0135-16}},
doi = {{10.2450/2016.0135-16}},
volume = {{16}},
year = {{2018}},
}