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Q41924751-715DBA6B-B281-4827-9F5C-671DC234725E
Q41924751-715DBA6B-B281-4827-9F5C-671DC234725E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41924751-715DBA6B-B281-4827-9F5C-671DC234725E
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy.
P2860
Q41924751-715DBA6B-B281-4827-9F5C-671DC234725E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41924751-715DBA6B-B281-4827-9F5C-671DC234725E
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wasDerivedFrom
d86e7132664b9d961e85547a118e83fbcc14f9c1
P2860
Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik.