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pro vyhledávání: '"D. S. Zanjani"'
Autor:
R. Mehrasa, Z. Badiei, M. E. Khayyami, M. Afzal Aghaee, D. S. Zanjani, M. Shahabi, A. Roodsarabi
Publikováno v:
Vox Sanguinis. 111:88-92
Background and objectives Bombay phenotype is characterized by the lack of H substance both on red blood cell (RBC) surface and in body secretions. Mutations of fucosyltransferase 1 (FUT1) and fucosyltransferase 2 (FUT2) genes are resulted in this ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::117fd8cdde19bef23b9f3cfd2136f99a
https://doi.org/10.1111/vox.12393
https://doi.org/10.1111/vox.12393
