Cita APA

Van de Sompele, S., PECHEUX, L., Couso, J., Meunier, A., Sanchez-Fernandez, M., & De Baere, E. (2017). Functional characterization of a novel non-coding mutation “Ghent +49A > G” in the iron-responsive element of L-ferritin causing hereditary hyperferritinaemia-cataract syndrome.

Citación estilo Chicago

Van de Sompele, Stijn, Lucie PECHEUX, Jorge Couso, Audrey Meunier, Mayka Sanchez-Fernandez, y Elfride De Baere. Functional Characterization of a Novel Non-coding Mutation “Ghent +49A > G” in the Iron-responsive Element of L-ferritin Causing Hereditary Hyperferritinaemia-cataract Syndrome. 2017.

Cita MLA

Van de Sompele, Stijn, et al. Functional Characterization of a Novel Non-coding Mutation “Ghent +49A > G” in the Iron-responsive Element of L-ferritin Causing Hereditary Hyperferritinaemia-cataract Syndrome. 2017.