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Molecular pathology and funct. genomics, 2019

DOI: 10.1183/13993003.congress-2019.pa4063

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Patients with Alpha-1 antitrypsin Deficiency due to Null mutations have clinical peculiarities and should require personalized pulmonary management

Proceedings article published in 2019 by Ilaria Ferrarotti, Stefania Ottaviani ORCID, Elena Paracchini, Davide Piloni, Francesca Mariani, Gregorino Paone, Alice M. Balderacchi, Valentina Barzon, Matteo Bosio, Zamir Kadija, Bruno Balbi ORCID, Angelo G. Corsico
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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