APA
Saunier C., Støve S. I., Popp B., Gérard B., Blenski M., AhMew N., de Bie C., Goldenberg P., Isidor B., Keren B., Leheup B., Lampert L., Mignot C., Tezcan K., Mancini G. M. S., Nava C., Wasserstein M., Bruel A., Thevenon J., Masurel A., Duffourd Y., Kuentz P., Huet F., Rivière J., van Slegtenhorst M., Faivre L., Piton A., Reis A., Arnesen T., Thauvin-Robinet C. & Zweier C. (20171215). Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency. : Human mutation.
Chicago
Saunier Chloé, Støve Svein Isungset, Popp Bernt, Gérard Bénédicte, Blenski Marina, AhMew Nicholas, de Bie Charlotte, Goldenberg Paula, Isidor Bertrand, Keren Boris, Leheup Bruno, Lampert Laetitia, Mignot Cyril, Tezcan Kamer, Mancini Grazia M S, Nava Caroline, Wasserstein Melissa, Bruel Ange-Line, Thevenon Julien, Masurel Alice, Duffourd Yannis, Kuentz Paul, Huet Frédéric, Rivière Jean-Baptiste, van Slegtenhorst Marjon, Faivre Laurence, Piton Amélie, Reis André, Arnesen Thomas, Thauvin-Robinet Christel and Zweier Christiane. 20171215. Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency. : Human mutation.
Harvard
Saunier C., Støve S. I., Popp B., Gérard B., Blenski M., AhMew N., de Bie C., Goldenberg P., Isidor B., Keren B., Leheup B., Lampert L., Mignot C., Tezcan K., Mancini G. M. S., Nava C., Wasserstein M., Bruel A., Thevenon J., Masurel A., Duffourd Y., Kuentz P., Huet F., Rivière J., van Slegtenhorst M., Faivre L., Piton A., Reis A., Arnesen T., Thauvin-Robinet C. and Zweier C. (20171215). Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency. : Human mutation.
MLA
Saunier Chloé, Støve Svein Isungset, Popp Bernt, Gérard Bénédicte, Blenski Marina, AhMew Nicholas, de Bie Charlotte, Goldenberg Paula, Isidor Bertrand, Keren Boris, Leheup Bruno, Lampert Laetitia, Mignot Cyril, Tezcan Kamer, Mancini Grazia M S, Nava Caroline, Wasserstein Melissa, Bruel Ange-Line, Thevenon Julien, Masurel Alice, Duffourd Yannis, Kuentz Paul, Huet Frédéric, Rivière Jean-Baptiste, van Slegtenhorst Marjon, Faivre Laurence, Piton Amélie, Reis André, Arnesen Thomas, Thauvin-Robinet Christel and Zweier Christiane. Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency. : Human mutation. 20171215.