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Q50296216-BF0A2CF0-0487-415C-9FCE-8DC4DC2FD6FF
Q50296216-BF0A2CF0-0487-415C-9FCE-8DC4DC2FD6FF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50296216-BF0A2CF0-0487-415C-9FCE-8DC4DC2FD6FF
SLC35A1 exchanges CMP-Neu5Ac for CMP
P2860
Q50296216-BF0A2CF0-0487-415C-9FCE-8DC4DC2FD6FF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50296216-BF0A2CF0-0487-415C-9FCE-8DC4DC2FD6FF
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wasDerivedFrom
88e468fb6a5208c5ad1413249410b3bd1fd6ed9e
P2860
Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter.