Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease

Por Payne, Felicity, Lim, Koini, Girousse, Amandine, Brown, Rebecca J., Kory, Nora, Robbins, Ann, Xue, Yali, Sleigh, Alison, Cochran, Elaine, Adams, Claire, Dev Borman, Arundhati, Russel-Jones, David, Gorden, Phillip, Semple, Robert K., Saudek, Vladimir, O’Rahilly, Stephen, Walther, Tobias C., Barroso, Inês, Savage, David B.
Publicado em 2014