PP6.6 – 1797 Isolated complex I deficiency and atypical clinical courses in three patients due to novel mutations in NDUFS1 and NDUFV1

K Björkman,K Sofou, N Darin, G Kollberg, E Holme, M Tulinius,A Oldfors,AR Moslemi

European Journal of Paediatric Neurology(2013)

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