Identification of a novel erythroid-specific enhancer for the ALAS2 gene and its loss-of-function mutation which is associated with congenital sideroblastic anemia.

Kaneko, Kiriko

Identification of a novel erythroid-specific enhancer for the ALAS2 gene and its loss-of-function mutation which is associated with congenital sideroblastic anemia. [electronic resource] - Haematologica Feb 2014 - 252-61 p. digital

Publication Type: Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't

1592-8721

10.3324/haematol.2013.085449 doi


5-Aminolevulinate Synthetase--genetics
Anemia, Sideroblastic--congenital
Enhancer Elements, Genetic
GATA1 Transcription Factor--genetics
Humans
K562 Cells
Male
Mutation
Response Elements