The molecular basis of hereditary complement factor I deficiency.

Eitemau Tebyg

• Molecular basis of hereditary C3 deficiency.
  gan: Botto, M, et al.
  Cyhoeddwyd: (1990)
• Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema.
  gan: Cicardi, M, et al.
  Cyhoeddwyd: (1987)
• Molecular characterization of homozygous hereditary factor I deficiency
  gan: BARACHO, G V, et al.
  Cyhoeddwyd: (2003)
• Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I).
  gan: Tanguay, R M, et al.
  Cyhoeddwyd: (1990)
• Hereditary deficiency of the fifth component of complement in man. I. Clinical, immunochemical, and family studies.
  gan: Rosenfeld, S I, et al.
  Cyhoeddwyd: (1976)