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...Prokisch H, Mayr JA, McFarland R, Poulton J, Ryan MT, Wittig I, Henneke M, Taylor RW (2018) Bi-allelic mutations in NDUFA6 establish its role in early-onset ...Prokisch H, Mayr JA, McFarland R, Poulton J, Ryan MT, Wittig I, Henneke M, Taylor RW

...McFarland R, Prokisch H, Wortmann SB, Bonnen PE, Wittig I, Pagliarini DJ, Taylor RW (2020) Pathogenic bi-allelic mutations in NDUFAF8 cause Leigh syndrome w ...McFarland R, Prokisch H, Wortmann SB, Bonnen PE, Wittig I, Pagliarini DJ, Taylor RW

...n found either in the mitochondrial or in the nuclear genome. Prognosis of LS is poor. The identification of molecular defect contributes to management a ...n found either in the mitochondrial or in the nuclear genome. Prognosis of LS is poor. The identification of molecular defect contributes to management a

...onchi D, Murayama K, Ohtake A, Rebelo-Guiomar P, Kohda M, Kang D, Mayr JA, Taylor RW, Okazaki Y, Minczuk M, Prokisch H (2017) Biallelic C1QBP mutations cause ...onchi D, Murayama K, Ohtake A, Rebelo-Guiomar P, Kohda M, Kang D, Mayr JA, Taylor RW, Okazaki Y, Minczuk M, Prokisch H

::::#Taylor KW, Novak RF, Anderson HA, Birnbaum LS, Blystone C, Devito M, Jacobs D, Köhrle J, Lee DH, Rylander L, Rignell-Hyd

...hi, M Greaves, P Vyas, AK El-Naggar, T Santarius, VP Collins, R Grundy, JA Taylor, DN Hayes, D Malkin, CS Foster, AY Warren, HC Whitaker, D Brewer, R Eeles, :::# JP Mazat, T Letellier, F Bedes, M Malgat, B Korzeniewski, LS Jouaville, R Morkuniene (1997). Metabolic control analysis and threshold ef

:::: '''1.21. Ref 65''' Fink BD, Bai F, Yu L, Sheldon RD, Sharma A, Taylor EB, Sivitz WI (2018) Oxaloacetic acid mediates ADP-dependent inhibition of :::: '''2.87. Ref 185''' Yépez VA, Kremer LS, Iuso A, Gusic M, Kopajtich R, Koňaříková E, Nadel A, Wachutka L, Proki