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Q40233943-90D28983-8CEA-4209-8293-A486345FE19A
Q40233943-90D28983-8CEA-4209-8293-A486345FE19A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40233943-90D28983-8CEA-4209-8293-A486345FE19A
A novel homozygous VPS45 p.P468L mutation leading to severe congenital neutropenia with myelofibrosis.
P1476
Q40233943-90D28983-8CEA-4209-8293-A486345FE19A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40233943-90D28983-8CEA-4209-8293-A486345FE19A
rank
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type
BestRank
Statement
wasDerivedFrom
536455116ab48e0cf5ae58674702912b21e58b3c
P1476
A novel homozygous VPS45 p.P46
......
eutropenia with myelofibrosis.
@en