8j0n | pdb_00008j0n
From Proteopedia
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 05:46, 3 April 2024.