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A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome

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The authors named this variant of Epitalon Ala Glu AspGly, which indicates a potential naming mistake

203 Despite this, advances in cancer mutation analysis and TCR sequencing have made it possible to assess whether an individual patient lacks the necessary TCRs to recognize crucial neoantigens

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