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FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon

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 (2018) In Blood Transfusion 16. p.101-104
Please use this url to cite or link to this publication:
author
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Blood Transfusion
volume
16
pages
101 - 104
publisher
SIMITI SERVIZI SRL
external identifiers
  • 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
2018-05-29 12:14:44
@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    = {SIMITI SERVIZI SRL},
  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},
  volume       = {16},
  year         = {2018},
}