Mitochondrial Changes in β(0)-Thalassemia/Hb E Disease

The compound β°-thalassemia/Hb E hemoglobinopathy is characterized by an unusually large range of presentation from essentially asymptomatic to a severe transfusion dependent state. While a number of factors are known that moderate presentation, these factors do not account for the full spectrum of...

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Dettagli Bibliografici
Pubblicato in:PLoS One
Autori principali: Khungwanmaythawee, Kornpat, Sornjai, Wannapa, Paemanee, Atchara, Jaratsittisin, Janejira, Fucharoen, Suthat, Svasti, Saovaros, Lithanatudom, Pathrapol, Roytrakul, Sittiruk, Smith, Duncan R.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Public Library of Science 2016
Soggetti:
Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4836671/
https://ncbi.nlm.nih.gov/pubmed/27092778
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0153831
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