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Q36649115-BA365B8F-A51E-4ABD-83CA-E5B9F1271C98
Q36649115-BA365B8F-A51E-4ABD-83CA-E5B9F1271C98
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36649115-BA365B8F-A51E-4ABD-83CA-E5B9F1271C98
Novel mutations in the ferritin-L iron-responsive element that only mildly impair IRP binding cause hereditary hyperferritinaemia cataract syndrome.
P6179
Q36649115-BA365B8F-A51E-4ABD-83CA-E5B9F1271C98
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36649115-BA365B8F-A51E-4ABD-83CA-E5B9F1271C98
rank
NormalRank
type
BestRank
Statement
P6179
1003278317
http://www.w3.org/2001/XMLSchema#string