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}},
}