APOB, apolipoprotein B, 338

N. diseases: 339; N. variants: 122
Disease: Ataxia with vitamin E deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1848533
Disease: Ataxia with vitamin E deficiency
Ataxia with vitamin E deficiency 		0.300 Biomarker disease CTD_human A novel delins mutation in the alpha-TTP gene in a family segregating ataxia with isolated vitamin E deficiency. 18458655 2008