A mutation in MT-TW causes a tRNA processing defect and reduced mitochondrial function in a family with Leigh syndrome.

Pubmed ID: 
26524491
Year: 
2015
Month: 
NOV
Volume: 
25
Citation: 
Duff RM, Shearwood AM, Ermer J, Rossetti G, Gooding R, Richman TR, Balasubramaniam S, Thorburn DR, Rackham O, Lamont PJ, Filipovska A. A mutation in MT-TW causes a tRNA processing defect and reduced mitochondrial function in a family with Leigh syndrome. Mitochondrion 25 : 113 - 9(2015) PubMed (Grant IDs: APP1058442, APP1045677, APP1041582, APP1023460, APP1005030)