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Q35064189-091C584E-4223-4897-AC80-8FEB261C097E
Q35064189-091C584E-4223-4897-AC80-8FEB261C097E
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http://www.wikidata.org/entity/statement/Q35064189-091C584E-4223-4897-AC80-8FEB261C097E
Whole-exome sequencing reveals overlap between macrophage activation syndrome in systemic juvenile idiopathic arthritis and familial hemophagocytic lymphohistiocytosis
P2860
Q35064189-091C584E-4223-4897-AC80-8FEB261C097E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35064189-091C584E-4223-4897-AC80-8FEB261C097E
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wasDerivedFrom
10c1579bee5f281015dd3dfe406389cead673b01
P2860
Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH.