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Q47813038-1A00C8D3-0F25-41D8-B798-A49BA6FF6CE1
Q47813038-1A00C8D3-0F25-41D8-B798-A49BA6FF6CE1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47813038-1A00C8D3-0F25-41D8-B798-A49BA6FF6CE1
Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights.
P2860
Q47813038-1A00C8D3-0F25-41D8-B798-A49BA6FF6CE1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47813038-1A00C8D3-0F25-41D8-B798-A49BA6FF6CE1
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
540fa72102be14f7463f360af811ba7d2d1de5a8
P2860
Neurodegeneration caused by proteins with an aberrant carboxyl-terminus.