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pubmed-article:15658192pubmed:abstractTextA new alpha-globin mutation causing persistent mild hypochromic microcytosis and erythrocytosis is described. Hb Zurich Albisrieden [alpha59(E8)Gly-->Arg (alpha2)] is not detected at the protein level and leads to alpha(+)-thalassemia (thal).lld:pubmed
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pubmed-article:15658192pubmed:articleTitleA new highly unstable alpha chain variant causing alpha(+)-thalassemia: Hb Zurich Albisrieden [alpha59(E8)Gly-->Arg (alpha2)].lld:pubmed
pubmed-article:15658192pubmed:affiliationInstitute for Medical and Molecular Diagnostics Ltd, Zürich, Switzerland.lld:pubmed
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