Recurrent macrophage activation syndrome associated with heterozygous perforin W374X gene mutation in a child with systemic juvenile idiopathic arthritis.


Unal Ş. , Balta G. , Okur H., Aytac S., Cetin M., Gumruk F., ...Daha Fazla

Journal of pediatric hematology/oncology, cilt.35, 2013 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier