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Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
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α(+)-Thalassemia trait caused by a frameshift mutation in exon 2 of the α2-globin gene [HBA2 c.244delT]

John S Waye1, Lynda Walker, Barry Eng

  • 1Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada. waye@hhsc.ca

Hemoglobin
|March 2, 2012
PubMed

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