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Severe α-1 antitrypsin deficiency caused by Q0(Ourém) allele: clinical features, haplotype characterization and

L Vaz Rodrigues1, F Costa, P Marques

  • 1Pulmonology Department, Centro Hospitalar de Coimbra, EPE, Coimbra, Portugal.

Clinical Genetics
|April 5, 2011
PubMed

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