Gene: UEVLD ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55293
Gene Symbol: UEVLD
UEVLD 		0.010 GeneticVariation phenotype BEFREE Since the neuromuscular deficits of ATTP-KO mice appear to be similar to those of patients with ATTP mutations, it is suggested that over-expression of sln and uchl1 may also contribute to AT-sensitive ataxia in humans. 19204867 2009