Cerebrocostomandibular-like syndrome and a mutation in the conserved oligomeric Golgi complex, subunit 1

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Oxford University Press

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COG8 deficiency causes new congenital disorder of glycosylation type IIh

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Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation

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A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1–Cog8 interaction in COG complex formation

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Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik

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