8s9s
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Structure of the human ER membrane protein complex (EMC) in GDN
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Structural highlights
DiseaseEMC1_HUMAN Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome. The disease is caused by mutations affecting the gene represented in this entry. FunctionContents | ||||||||||||||||||
This page was last modified 07:03, 18 May 2023.