Human Genome Epidemiology Literature Finder
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Query Trace: Epilepsy and SUCLG1[original query] |
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Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients. Journal of inherited metabolic disease 2015 Oct . Carrozzo Rosalba, Verrigni Daniela, Rasmussen Magnhild, de Coo Rene, Amartino Hernan, Bianchi Marzia, Buhas Daniela, Mesli Samir, Naess Karin, Born Alfred Peter, Woldseth Berit, Prontera Paolo, Batbayli Mustafa, Ravn Kirstine, Joensen Fróði, Cordelli Duccio M, Santorelli Filippo Maria, Tulinius Mar, Darin Niklas, Duno Morten, Jouvencel Philippe, Burlina Alberto, Stangoni Gabriela, Bertini Enrico, Redonnet-Vernhet Isabelle, Wibrand Flemming, Dionisi-Vici Carlo, Uusimaa Johanna, Vieira Paivi, Osorio Andrés Nascimento, McFarland Robert, Taylor Robert W, Holme Elisabeth, Ostergaard Elseb |
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