Alpha 1 antitrypsin deficiency (AATD) is an autosomal codominant genetic condition that affects Caucasians of the European population due to the presence of a deficient allele of the SERPINA1 gene. A frequency of about 1/5,000 individuals has been estimated in Italy.

Distribution of the Clinical Manifestations of Alpha 1 Antitrypsin Deficiency in Respiratory Outpatients from an Area of Northern Italy / Aiello, Marina; Marchi, Laura; Ferrarotti, Ilaria; Frizzelli, Annalisa; Pisi, Roberta; Calzetta, Luigino; Manari, Gaia; Pela', Giovanna Maria; Russo, Annalisa; Minerba, Roberta; Aloe, Rosalia; Ranzieri, Silvia; Corradi, Massimo; Chetta, Alfredo. - In: RESPIRATION. - ISSN 0025-7931. - (2022), pp. 1-8. [10.1159/000525549]

Distribution of the Clinical Manifestations of Alpha 1 Antitrypsin Deficiency in Respiratory Outpatients from an Area of Northern Italy

Aiello, Marina;Marchi, Laura;Frizzelli, Annalisa;Pisi, Roberta;Calzetta, Luigino;Manari, Gaia;Pela' Giovanna Maria;Ranzieri, Silvia;Corradi, Massimo;Chetta, Alfredo
2022

Abstract

Alpha 1 antitrypsin deficiency (AATD) is an autosomal codominant genetic condition that affects Caucasians of the European population due to the presence of a deficient allele of the SERPINA1 gene. A frequency of about 1/5,000 individuals has been estimated in Italy.
Distribution of the Clinical Manifestations of Alpha 1 Antitrypsin Deficiency in Respiratory Outpatients from an Area of Northern Italy / Aiello, Marina; Marchi, Laura; Ferrarotti, Ilaria; Frizzelli, Annalisa; Pisi, Roberta; Calzetta, Luigino; Manari, Gaia; Pela', Giovanna Maria; Russo, Annalisa; Minerba, Roberta; Aloe, Rosalia; Ranzieri, Silvia; Corradi, Massimo; Chetta, Alfredo. - In: RESPIRATION. - ISSN 0025-7931. - (2022), pp. 1-8. [10.1159/000525549]
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11381/2927551
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