Milger, K., Holdt, L. M., Teupser, D., Huber, R. M., Behr, J., & Kneidinger, N. (2015). Identification of a novel SERPINA-1 mutation causing alpha-1 antitrypsin deficiency in a patient with severe bronchiectasis and pulmonary embolism. Int J Chron Obstruct Pulmon Dis.
Chicago Style aipamenaMilger, Katrin, Lesca Miriam Holdt, Daniel Teupser, Rudolf Maria Huber, Jürgen Behr, and Nikolaus Kneidinger. "Identification of a Novel SERPINA-1 Mutation Causing Alpha-1 Antitrypsin Deficiency in a Patient With Severe Bronchiectasis and Pulmonary Embolism." Int J Chron Obstruct Pulmon Dis 2015.
MLA aipamenaMilger, Katrin, et al. "Identification of a Novel SERPINA-1 Mutation Causing Alpha-1 Antitrypsin Deficiency in a Patient With Severe Bronchiectasis and Pulmonary Embolism." Int J Chron Obstruct Pulmon Dis 2015.