APA

van Well G. T. J., Kant B., van Nistelrooij A., Sirma Ekmekci S., Henriet S. V., Hoppenreijs E., van Deuren M., van Montfrans J., Nierkens S., Gül A. & van Gijn M. E. (20200108). Phenotypic variability including Behçet's disease-like manifestations in DADA2 patients due to a homozygous c.973-2A>G splice site mutation. : Clinical and experimental rheumatology.

Chicago

van Well Gijs T J, Kant Benjamin, van Nistelrooij Annabel, Sirma Ekmekci Sema, Henriet Stefanie V, Hoppenreijs Esther, van Deuren Marcel, van Montfrans Joris, Nierkens Stefan, Gül Ahmet and van Gijn Mariëlle E. 20200108. Phenotypic variability including Behçet's disease-like manifestations in DADA2 patients due to a homozygous c.973-2A>G splice site mutation. : Clinical and experimental rheumatology.

Harvard

van Well G. T. J., Kant B., van Nistelrooij A., Sirma Ekmekci S., Henriet S. V., Hoppenreijs E., van Deuren M., van Montfrans J., Nierkens S., Gül A. and van Gijn M. E. (20200108). Phenotypic variability including Behçet's disease-like manifestations in DADA2 patients due to a homozygous c.973-2A>G splice site mutation. : Clinical and experimental rheumatology.

MLA

van Well Gijs T J, Kant Benjamin, van Nistelrooij Annabel, Sirma Ekmekci Sema, Henriet Stefanie V, Hoppenreijs Esther, van Deuren Marcel, van Montfrans Joris, Nierkens Stefan, Gül Ahmet and van Gijn Mariëlle E. Phenotypic variability including Behçet's disease-like manifestations in DADA2 patients due to a homozygous c.973-2A>G splice site mutation. : Clinical and experimental rheumatology. 20200108.