Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ahmed Maded Al Harbi"'
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 3, Pp 132-134 (2020)
Leukocyte adhesion deficiency type II (LAD II) is a rare hereditary disorder caused by the mutation in the guanosine diphosphate-fucose transporter gene (SLC35C1). LAD II is characterized by inexpression of ABO antigens (i.e., Bombay phenotype) and t
Externí odkaz:
https://doaj.org/article/2d7f26ecbe5a410780e852360f0b066b
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 3, Pp 132-134 (2020)
Leukocyte adhesion deficiency type II (LAD II) is a rare hereditary disorder caused by the mutation in the guanosine diphosphate-fucose transporter gene (SLC35C1). LAD II is characterized by inexpression of ABO antigens (i.e., Bombay phenotype) and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::188230b98ffb81e03cbe4f0d1e26f8ef
http://www.jahjournal.org/article.asp?issn=1658-5127
http://www.jahjournal.org/article.asp?issn=1658-5127