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pro vyhledávání: '"Hb Adrian"'
Publikováno v:
Thalassemia Reports, Vol 13, Iss 2, Pp 152-156 (2023)
Background: Alpha thalassemia is one of the most common human genetic abnormalities. More than 400 different variations of the α-globin protein have been introduced, most of which are not associated with noticeable clinical manifestations. The ident
Externí odkaz:
https://doaj.org/article/e013d06df19d43399078244ed7af8d84