Disease: Congenital Myasthenic Syndromes, Postsynaptic ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751883
Disease: Congenital Myasthenic Syndromes, Postsynaptic
Congenital Myasthenic Syndromes, Postsynaptic 		0.300 Biomarker disease CTD_human GFPT1 deficiency in muscle leads to myasthenia and myopathy in mice. 29905857 2018