Sanger sequencing solved a cryptic case of severe alpha₁-antitrypsin deficiency. [electronic resource]
- Clinical biochemistry Apr 2012
- 499-501 p. digital
Publication Type: Case Reports; Journal Article
1873-2933
10.1016/j.clinbiochem.2012.01.027 doi
Genetic Association Studies Genotype Humans Male Middle Aged Mutation, Missense Pedigree Pulmonary Disease, Chronic Obstructive--diagnostic imaging Pulmonary Emphysema--diagnostic imaging Radiography Sequence Analysis, DNA alpha 1-Antitrypsin--genetics alpha 1-Antitrypsin Deficiency--complications