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APA Citation
Arostegui, J., Rabionet, R., Remesal, A., Mensa-Vilaro, A., Murias, S., Alcobendas, R., Gonzalez-Roca, E., Dreschsel, O., Ruiz-Ortiz, E., Puig, A., Comas, D., Ossowski, S., Yagüe, J., Estivill, X., & Merino, R. (2015). a family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis. Pediatric rheumatology online journal, 13(1), 1–2. http://access.bl.uk/ark:/81055/vdc_100080434504.0x000450