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Every 2 years since 1978, an international group of scientists, physicians, and other researchers meet to discuss the latest developments in the underlying etiology, mechanisms of action, and developmental acquisition of cellular and systemic defects exhibited and elicited by the most common inherited human disorders, the hemoglobinopathies. The 19th Hemoglobin Switching Conference, held in September 2014 at St. John's College in Oxford, once again exceeded all expectations by describing cutting edge research in cellular, molecular, developmental, and genomic advances focused on these diseases. The conference comprised about 60 short talks over 3 days by leading investigators in the field. This meeting report describes the highlights of the conference.

Original publication

DOI

10.1016/j.exphem.2015.06.008

Type

Journal article

Journal

Exp Hematol

Publication Date

10/2015

Volume

43

Pages

821 - 837

Keywords

Congresses as Topic, Hemoglobinopathies, Hemoglobins, Humans