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HAEMATOL.2013.085449
HAEMATOL.2013.085449
http://dx.doi.org/10.3324/HAEMATOL.2013.085449
Identification of a novel erythroid-specific enhancer for the ALAS2 gene and its loss-of-function mutation which is associated with congenital sideroblastic anemia.
P356
Q41813591-FAA176D7-88D0-4AFD-8E4F-3798EC6C2AE6
P356
HAEMATOL.2013.085449
http://dx.doi.org/10.3324/HAEMATOL.2013.085449