Characterization of the molecular basis of the alpha 1-antitrypsin F allele.

Antzeko izenburuak

• Molecular basis of alpha 1-antitrypsin deficiency and emphysema associated with the alpha 1-antitrypsin Mmineral springs allele.
  nork: Curiel, D T, et al.
  Argitaratua: (1990)
• Characterization of the gene and protein of the common alpha 1-antitrypsin normal M2 allele.
  nork: Nukiwa, T, et al.
  Argitaratua: (1988)
• Characterization of the normal alpha 1-antitrypsin allele Vmunich: a variant associated with a unique protein isoelectric focusing pattern.
  nork: Holmes, M D, et al.
  Argitaratua: (1990)
• Alpha 1-antitrypsin Null(isola di procida): an alpha 1-antitrypsin deficiency allele caused by deletion of all alpha 1-antitrypsin coding exons.
  nork: Takahashi, H, et al.
  Argitaratua: (1990)
• Alpha 1-antitrypsin deficiency caused by the alpha 1-antitrypsin Nullmattawa gene. An insertion mutation rendering the alpha 1-antitrypsin gene incapable of producing alpha 1-antitrypsin.
  nork: Curiel, D, et al.
  Argitaratua: (1989)