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Q36649115-39295287-E352-47D2-ACE8-40A6E41E7DB1
Q36649115-39295287-E352-47D2-ACE8-40A6E41E7DB1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36649115-39295287-E352-47D2-ACE8-40A6E41E7DB1
Novel mutations in the ferritin-L iron-responsive element that only mildly impair IRP binding cause hereditary hyperferritinaemia cataract syndrome.
P2860
Q36649115-39295287-E352-47D2-ACE8-40A6E41E7DB1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36649115-39295287-E352-47D2-ACE8-40A6E41E7DB1
rank
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type
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Statement
wasDerivedFrom
1fa686070c78162ae83feec3ace936dac5d6f686
P2860
Hyperferritinaemia-cataract syndrome: worldwide mutations and phenotype of an increasingly diagnosed genetic disorder.