Bi‐allelic pathogenic variants in NDUFC2 cause early‐onset Leigh syndrome and stalled biogenesis of complex I by Ahmad Alahmad, Alessia Nasca, Juliana Heidler, Kyle Thompson, Monika Oláhová, Andrea Legati, Eleonora Lamantea, Jana Meisterknecht, Manuela Spagnolo, Langping He, Seham Alameer, Fahad Hakami, Abeer Almehdar, Anna Ardissone, Charlotte L Alston, Robert McFarland, Ilka Wittig, Daniele Ghezzi, Robert W Taylor

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Impact of a NDUFC2 Variant on the Occurrence of Acute Coronary Syndromes by Giovanna Gallo, Serena Migliarino, Maria Cotugno, Rosita Stanzione, Simone Burocchi, Franca Bianchi, Simona Marchitti, Camillo Autore, Massimo Volpe, Speranza Rubattu, Speranza Rubattu

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Polymorphic variants at NDUFC2, encoding a mitochondrial complex I subunit, associate with cardiac hypertrophy in human hypertension by Giovanna Gallo, Maurizio Forte, Maria Cotugno, Simona Marchitti, Rosita Stanzione, Giuliano Tocci, Franca Bianchi, Silvia Palmerio, Mariarosaria Scioli, Giacomo Frati, Sebastiano Sciarretta, Emanuele Barbato, Massimo Volpe, Speranza Rubattu

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Ndufc2 Gene Inhibition Is Associated With Mitochondrial Dysfunction and Increased Stroke Susceptibility in an Animal Model of Complex Human Disease by Speranza Rubattu, Sara Di Castro, Herbert Schulz, Aron M. Geurts, Maria Cotugno, Franca Bianchi, Henrike Maatz, Oliver Hummel, Samreen Falak, Rosita Stanzione, Simona Marchitti, Stefania Scarpino, Betti Giusti, Ada Kura, Gian Franco Gensini, Flora Peyvandi, Pier Mannuccio Mannucci, Maurizia Rasura, Sebastiano Sciarretta, Melinda R. Dwinell, Norbert Hubner, Massimo Volpe

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