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COG1, 1-BP INS, 2659C

National Institutes of Health

Related topics

Related topics

1 relation
Congenital disorder of glycosylation, type 2G

Papers overview

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2017
2017
Hypothesis: lobe A (COG1–4)-CDG causes a more severe phenotype than lobe B (COG5–8)-CDG
The conserved oligomeric Golgi (COG) complex consists of eight subunits organized in two lobes: lobe A (COG1–4) and lobe B (COG5… 
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