Gene: FBXO38 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 81545
Gene Symbol: FBXO38
FBXO38 		0.300 GermlineCausalMutation disease ORPHANET A dominant mutation in FBXO38 causes distal spinal muscular atrophy with calf predominance. 24207122 2013