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Q33396841-7E83FFDF-0497-4778-9E60-997ADEA75E6E
Q33396841-7E83FFDF-0497-4778-9E60-997ADEA75E6E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33396841-7E83FFDF-0497-4778-9E60-997ADEA75E6E
A novel type of macrothrombocytopenia associated with a defect in α2,3-sialylation.
P2860
Q33396841-7E83FFDF-0497-4778-9E60-997ADEA75E6E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33396841-7E83FFDF-0497-4778-9E60-997ADEA75E6E
rank
NormalRank
type
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Statement
wasDerivedFrom
daa46ea477cb063f9ab4e4f6ec6cbafcd170416a
P2860
Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter.