Identification of a novel alpha1-antitrypsin variant
Alpha-1-antitrypsin deficiency (A1ATD) is a genetic condition caused by SERPINA1 mutations, which results into decreased protease inhibitor activity in the serum and predisposes to emphysema and/or to liver disease due to accumulation of the abnormal protein in the hepatic cells. In most cases the c...
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Bibliographic Details
| Main Authors: |
de Seynes, Camille,
Ged, C.,
de Verneuil, H.,
Chollet, N.,
Balduyck, M.,
Raherison, C. |
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| Format: | Online
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| Language: | English |
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| Published: |
Elsevier
2016
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198725/
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