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pro vyhledávání: '"Benjamin A. Barasa"'
Autor:
Brigitte A. van Oirschot, Benjamin A. Barasa, Richard van Wijk, Paola Bianchi, Wouter W. van Solinge, Monique Slijper, Albert J. R. Heck
Publikováno v:
Proteomics, 10(8), 859. Wiley-VCH Verlag
Purpose To date it still remains a challenge to correctly and timely diagnose red blood cell (RBC) enzymopathies that result in hereditary non-spherocytic hemolytic anemia, the third most common of which is pyrimidine 5’-nucleotidase (P5N) deficien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cc65e881def32affc54e89661e6c0d9
https://dspace.library.uu.nl/handle/1874/356939
https://dspace.library.uu.nl/handle/1874/356939