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Q37671886-02DAE502-21F2-48F6-B2BE-8339F3E81487
Q37671886-02DAE502-21F2-48F6-B2BE-8339F3E81487
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37671886-02DAE502-21F2-48F6-B2BE-8339F3E81487
Metabolism, cell surface organization, and disease.
P2860
Q37671886-02DAE502-21F2-48F6-B2BE-8339F3E81487
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37671886-02DAE502-21F2-48F6-B2BE-8339F3E81487
rank
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Statement
wasDerivedFrom
cc73883777e96d2a746a0d1ffc92222268810137
P2860
Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development