PVALB, parvalbumin, 5816

N. diseases: 148; N. variants: 0
Disease: Friedreich Ataxia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0016719
Disease: Friedreich Ataxia
Friedreich Ataxia 		0.010 GeneticVariation disease BEFREE Here, we report a new conditional mouse model with complete frataxin deletion in parvalbumin-positive cells that recapitulate the sensory ataxia and neuropathy associated to FA, albeit with a more rapid and severe course. 29853274 2018