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Q28704337-17F2A8F4-90C9-408F-A8F6-FEC6A010CC5C
Q28704337-17F2A8F4-90C9-408F-A8F6-FEC6A010CC5C
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http://www.wikidata.org/entity/statement/Q28704337-17F2A8F4-90C9-408F-A8F6-FEC6A010CC5C
GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome
P2860
Q28704337-17F2A8F4-90C9-408F-A8F6-FEC6A010CC5C
BestRank
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http://www.wikidata.org/entity/statement/Q28704337-17F2A8F4-90C9-408F-A8F6-FEC6A010CC5C
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wasDerivedFrom
572f71be7af926a04867b054951183af4e8264b8
P2860
Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency.