Severe autoinflammatory disease caused by mutation in a gene controlling actin cytoskeletal dynamics and cure with allogeneic haematopoetic stem cell transplantation

مواد مشابهة

• Actin cytoskeletal defects in immunodeficiency
  بواسطة: Moulding, Dale A, وآخرون
  منشور في: (2013)
• Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1
  بواسطة: Standing, Ariane S.I., وآخرون
  منشور في: (2017)
• Identification of a novel monogenic autoinflammatory disease due to mutation in a mitochondrial chaperone protein in a single kindred, and cure with allogeneic haematopoietic stem cell transplantation
  بواسطة: Standing, Ariane, وآخرون
  منشور في: (2014)
• Monogenic polyarteritis nodosa caused by ADA2 Deficiency: the GOSH experience
  بواسطة: Nanthapisal, S, وآخرون
  منشور في: (2015)
• Loss of function mutation in a mitochondrial chaperone protein leading to dyregulated ROS production, and autoinflammatory disease in a single kindred
  بواسطة: Standing, A, وآخرون
  منشور في: (2015)