Complementarity of electrophoretic, mass spectrometric, and gene sequencing techniques for the diagnosis and characterization of congenital disorders of glycosylation

MLA

Marie-Line Jacquemont, et al. “Complementarity of Electrophoretic, Mass Spectrometric, and Gene Sequencing Techniques for the Diagnosis and Characterization of Congenital Disorders of Glycosylation.” Electrophoresis, vol. 39, no. 24, Jan. 2018. EBSCOhost, https://doi.org/10.1002/elps.201800021⟩.

APA

Marie-Line Jacquemont, Nathalie Seta, Valérie Drouin-Garraud, François Fenaille, André Mégarbané, Arnaud Bruneel, David Cheillan, Coralie Ruel, Sandrine Vuillaumier-Barrot, Thierry Dupré, Aline Cano, & Sophie Cholet. (2018). Complementarity of electrophoretic, mass spectrometric, and gene sequencing techniques for the diagnosis and characterization of congenital disorders of glycosylation. Electrophoresis, 39(24). https://doi.org/10.1002/elps.201800021⟩

Chicago

Marie-Line Jacquemont, Nathalie Seta, Valérie Drouin-Garraud, François Fenaille, André Mégarbané, Arnaud Bruneel, David Cheillan, et al. 2018. “Complementarity of Electrophoretic, Mass Spectrometric, and Gene Sequencing Techniques for the Diagnosis and Characterization of Congenital Disorders of Glycosylation.” Electrophoresis 39 (24). doi:10.1002/elps.201800021⟩.