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

Valeria Tiranti(Istituto Nazionale Genetica Molecolare), Konstanze Hoertnagel(Ludwig-Maximilians-Universität München), Rosalba Carrozzo(Bambino Gesù Children's Hospital), C. Galimberti(Fondazione IRCCS Istituto Neurologico Carlo Besta), M. Munaro(Fondazione IRCCS Istituto Neurologico Carlo Besta), Matteo Granatiero(Casa Sollievo della Sofferenza), Leopoldo Zelante(Casa Sollievo della Sofferenza), Paolo Gasparini(Casa Sollievo della Sofferenza), R. Marzella(University of Bari Aldo Moro), Mariano Rocchi(University of Bari Aldo Moro), M. Pilar Bayona‐Bafaluy(Universidad de Zaragoza), José Antonio Enrı́quez(Universidad de Zaragoza), Graziella Uziel(Fondazione IRCCS Istituto Neurologico Carlo Besta), Enrico Bertini(Bambino Gesù Children's Hospital), Carlo Dionisi‐Vici(Bambino Gesù Children's Hospital), Brunella Franco(Telethon Institute Of Genetics And Medicine), Thomas Meitinger(Ludwig-Maximilians-Universität München), Massimo Zeviani(Fondazione IRCCS Istituto Neurologico Carlo Besta)
The American Journal of Human Genetics
December 1, 1998
Cited by 528Open Access
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