Singhi, P., De Meirleir, L., Lissens, W., Singhi, S., & Saini, A. G. (2013). Pyruvate Dehydrogenase-E1α Deficiency Presenting as Recurrent Demyelination: An Unusual Presentation and a Novel Mutation. Springer Berlin Heidelberg.
Citação norma ChicagoSinghi, Pratibha, Linda De Meirleir, Willy Lissens, Sunit Singhi, and Arushi Gahlot Saini. Pyruvate Dehydrogenase-E1α Deficiency Presenting As Recurrent Demyelination: An Unusual Presentation and a Novel Mutation. Springer Berlin Heidelberg, 2013.
Citação norma MLASinghi, Pratibha, et al. Pyruvate Dehydrogenase-E1α Deficiency Presenting As Recurrent Demyelination: An Unusual Presentation and a Novel Mutation. Springer Berlin Heidelberg, 2013.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.