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Published in 2020 at "Journal of the Neurological Sciences"
DOI: 10.1016/j.jns.2019.116562
Abstract: The m.3243A > G mutation in the mitochondrial tRNALeu (UUR) gene is associated with a variety of phenotypic heterogeneity. The clinical spectrum and phenotypic-genotypic correlations in the Chinese patients are poorly understood. In the present study, we…
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Keywords:
mutation;
mitochondrial trnaleu;
seven han;
trnaleu uur ... See more keywords