Hematologically Important Mutations: The Autosomal Recessive Forms of Chronic Granulomatous Disease (First Update)

This publication has 23 references indexed in Scilit:

• Chronic Granulomatous Disease: Report on a National Registry of 368 Patients
  Medicine, 2000
• Genetic, Biochemical, and Clinical Features of Chronic Granulomatous Disease
  Medicine, 2000
• Recombination events between the p47-phoxgene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease
  Blood, 2000
• Hematologically Important Mutations: X-Linked Chronic Granulomatous Disease—An Update
  Blood Cells, Molecules, and Diseases, 1997
• A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease.
  Journal of Clinical Investigation, 1997
• Hematologically Important Mutations: The Autosomal Recessive Forms of Chronic Granulomatous Disease
  Blood Cells, Molecules, and Diseases, 1996
• Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease
  Blood, 1996
• Homologous Dinucleotide (GT or TG) Deletion in Japanese Patients with Chronic Granulomatous Disease with p47-Phox Deficiency
  Biochemical and Biophysical Research Communications, 1994
• In vitro molecular reconstitution of the respiratory burst in B lymphoblasts from p47-phox-deficient chronic granulomatous disease.
  Journal of Clinical Investigation, 1993
• Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat.
  Proceedings of the National Academy of Sciences, 1991