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1750-1172-8-30
1750-1172-8-30
http://dx.doi.org/10.1186/1750-1172-8-30
Novel mutations in the ferritin-L iron-responsive element that only mildly impair IRP binding cause hereditary hyperferritinaemia cataract syndrome.
P356
Q36649115-8B948478-0E9F-4BB5-A74B-142320A9A827
P356
1750-1172-8-30
http://dx.doi.org/10.1186/1750-1172-8-30