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Screening for Alpha 1 antitrypsin deficiency in Tunisian subjects with obstructive lung disease: a feasibility report

By Sabri Denden, Michele Zorzetto, Fethi Amri, Jalel Knani, Stefania Ottaviani, Roberta Scabini, Marina Gorrini, Ilaria Ferrarotti, Ilaria Campo, Jemni Ben Chibani, Amel Haj Khelil and Maurizio Luisetti
Topics: Research
Publisher: BioMed Central
OAI identifier: oai:pubmedcentral.nih.gov:2672056
Provided by: PubMed Central
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    Citations

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    2. (2004). Parfrey H: Alpha 1 Antitrypsin deficiency 4: molecular pathophysiology. Thorax
    3. (2005). Prevalence and phenotype of subjects carrying rare variants in the Italian registry for alpha1-antitrypsin deficiency.
    4. (2008). Wielders JPM: Inherited obstructive pulmonary disease: new selective sequencing workup for α1-antitrypsin deficiency identified two previously unidentified Null allels. Clin Chem
    5. (1990). α1-antitrypsin Deficiency, emphysema, and liver disease genetic basis and strategies for therapy.

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