✦ LIBER ✦

Leigh syndrome associated with mitochondrial complex I deficiency due to novel mutations In NDUFV1 and NDUFS2

✍ Scribed by Marin, Samantha E.; Mesterman, Ronit; Robinson, Brian; Rodenburg, Richard J.; Smeitink, Jan; Tarnopolsky, Mark A.

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A novel NDUFV1 gene mutation in complex

✍ C Vilain; C Rens; A Aeby; D Balériaux; P Van Bogaert; G Remiche; J Smet; R Van C 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 748 KB

A novel mutation in the human complex I

✍ Sophie Lebon; Diana Rodriguez; Delphine Bridoux; Amal Zerrad; Agnès Rötig; Arnol 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 310 KB

A catalytic defect in mitochondrial resp

✍ Lock Hock Ngu; Leo G. Nijtmans; Felix Distelmaier; Hanka Venselaar; Sjenet E. va 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 867 KB

PP6.6 – 1797 Isolated complex I deficien

✍ Björkman, K; Sofou, K; Darin, N; Kollberg, G; Holme, E; Tulinius, M; Oldfors, A; 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 61 KB

MLP027 Serial magnetic resonance imaging

✍ D. Zafeiriou; R.J.T. Rodenburg; H. Scheffer; L.P. van den Heuvel; F. Athanasiado 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 42 KB

P182 – 1614 Mitochondrial Complex I defi

✍ Arslan, M; Aydin, HI; Vurucu, S; Ünay, B; Gül, D; Akin, R 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 68 KB