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Q24337849-C17A6313-EAC8-4F06-AC24-5187D069C84D
Q24337849-C17A6313-EAC8-4F06-AC24-5187D069C84D
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Statement
http://www.wikidata.org/entity/statement/Q24337849-C17A6313-EAC8-4F06-AC24-5187D069C84D
Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation
P2860
Q24337849-C17A6313-EAC8-4F06-AC24-5187D069C84D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24337849-C17A6313-EAC8-4F06-AC24-5187D069C84D
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wasDerivedFrom
c047358b67074145a6cd92692bfff2f9e36dd9ab
P2860
Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency.