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Hb H disease in a Turkish family resulting from the interaction of a deletional α-thalassaemia-1 and a newly discovered poly A mutation

✍ Scribed by G. T. Yuuregir; K. Aksoy; M. A. ÇUuruuk; N. Dikmen; Y.-J. Fei; E. Baysal; T. H. J. Huisman

No coin nor oath required. For personal study only.

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