Joint Shantou International Eye Centre of Shantou University and The Chinese University of Hong Kong

By gene
  
By phenotype
  



Gene : DPAGT1
    
OMIM : 191350
    
UniProt : Q9H3H5
    
AmiGO : Q9H3H5
    
Phenotype : Congenital disorder of glycosylation, type Ij Myasthenic syndrome, congenital, 13, with tubular aggregates