Mutations of SURF-1 in Leigh Disease Associated with Cytochrome c Oxidase Deficiency

The American Journal of Human Genetics - Tập 63 Số 6 - Trang 1609-1621 - 1998
Valeria Tiranti1, Konstanze Hoertnagel2, Rosalba Carrozzo3, Claudia Galimberti1, M. Munaro1, Matteo Granatiero4, Leopoldo Zelante4, Paolo Gasparini4, R. Marzella5, Mariano Rocchi5, M. Pilar Bayona‐Bafaluy6, José Antonio Enrı́quez6, Graziella Uziel1, Enrico Bertini3, Carlo Dionisi‐Vici3, Brunella Franco7, Thomas Meitinger2, Massimo Zeviani1
1Istituto Nazionale Neurologico Carlo Besta
2Abteilung Medizinische Genetik, Kinderklinik der Ludwig-Maximilians Universität München, Munich
3Ospedale Pediatrico Bambino Gesù, Rome
4Casa sollievo della sofferenza, S Giovanni Rotondo, Italy
5Università Statale di Bari, Bari, Italy
6Universidad de Zaragoza, Zaragoza, Spain
7Téléthon Institute for Genetics and Medicine, Milan

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