Impaired activity of CCA-adding enzyme TRNT1 impacts OXPHOS complexes and cellular respiration in SIFD patient-derived fibroblasts

Overview of attention for article published in Orphanet Journal of Rare Diseases, June 2016

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Now That I'm Here, 20 Jun 2016

Last Saturday, Orphanet Journal of Rare Diseases published a paper on TRNT1 deficiency, the gene defect that causes SIFD, Kate's…

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