Congenital analbuminemia attributable to compound heterozygosity for novel mutations in the albumin gene

Clin Chem. 2005 Jul;51(7):1256-8. doi: 10.1373/clinchem.2005.048561.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Blood Protein Disorders / congenital
  • Blood Protein Disorders / genetics
  • Heterozygote
  • Humans
  • Male
  • Mutation
  • Polymorphism, Restriction Fragment Length
  • Polymorphism, Single-Stranded Conformational
  • Serum Albumin / deficiency*
  • Serum Albumin / genetics*

Substances

  • Serum Albumin