Emphysema associated with complete absence of alpha 1- antitrypsin in serum and the homozygous inheritance [corrected] of a stop codon in an alpha 1-antitrypsin-coding exon.

Lignende værker

• Evaluation of "at risk" alpha 1-antitrypsin genotype SZ with synthetic oligonucleotide gene probes.
  af: Nukiwa, T, et al.
  Udgivet: (1986)
• Homozygous and heterozygous alpha-1-antitrypsin deficiency: prevalence in pulmonary emphysema.
  af: Hutchison, D. C.
  Udgivet: (1976)
• 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.
  af: Curiel, D, et al.
  Udgivet: (1989)
• Alpha 1-antitrypsin Null(isola di procida): an alpha 1-antitrypsin deficiency allele caused by deletion of all alpha 1-antitrypsin coding exons.
  af: Takahashi, H, et al.
  Udgivet: (1990)
• Characterization of the gene and protein of the common alpha 1-antitrypsin normal M2 allele.
  af: Nukiwa, T, et al.
  Udgivet: (1988)