Peripheral neuropathy and cognitive impairment associated with a novel monoallelic HARS variant.
Béryl Royer-BertrandPinelopi TsouniPatrick MullenBelinda Campos XavierLauréane Mittaz CrettolAlexander J LobrinusJoseph GhikaMatthias R BaumgartnerCarlo RivoltaAndrea Superti-FurgaThierry KuntzerChristopher FrancklynChristel TranPublished in: Annals of clinical and translational neurology (2019)
Genetic variants in the genes coding for the different aminoacyl-tRNA synthases are associated with various clinical conditions. To date, a number of HARS variant have been associated with peripheral neuropathy, but not cognitive deficits. Further studies are needed to explore why HARS mutations confer a neuronal-specific phenotype.