ERLIN1, ER lipid raft associated 1, 10613

N. diseases: 33; N. variants: 7
Disease: Amyotrophic Lateral Sclerosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.010 GeneticVariation disease BEFREE ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree. 29453415 2018