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Our mission is to identify those affected by alpha-1-antitrypsin deficiency and to improve the quality of their lives through support, education, advocacy and research. Alpha-1 is a genetic, inherited condition that may cause lung, liver or skin disease in affected individuals.

Describes the natural history, incidence and prevalence of cirrhosis and hepatocellular carcinoma in patients with homo- and heterozygote disease

Prof David Lomas

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Alpha-1 Antitrypsin Deficiency

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