[Acquisition of the wobble modification in another isoacceptor tRNA is critical for suppressing the MELAS mutation, highlighting the primary role of the UUG decoding deficiency in the molecular pathogenesis of MELAS syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE