Mutations in the<i>SURF1</i>gene associated with Leigh syndrome and cytochrome<i>c</i>oxidase deficiency

Human Mutation - Tập 17 Số 5 - Trang 374-381 - 2001
Marie O. Péquignot1, Runu Dey1, Massimo Zeviani2, Valeria Tiranti2, Catherine Godinot3, Alain Poyau3, Carolyn M. Sue4, Salvatore Di Mauro4, Marc Abitbol1, C Marsac1
1Laboratoire CERTO, Faculté Necker, Paris, France and CNRS UPR1524, Meudon, France
2Instituto Nazionale Neurologico “Carlo Besta”, Milan, Italy
3CNRS UMR 5534, Université Claude Bernard de Lyon, Villeurbanne, France
4Department of Neurology, Columbia University, New York, New York

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