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α(1)-Antitrypsin deficiency · 6: New and emerging treatments for α(1)-antitrypsin deficiency

Alpha-1-antitrypsin (AAT) deficiency is a genetic condition that increases the risk of developing lung and liver disease, as well as other associated conditions. Most treatment of affected individuals is not specifically directed at AAT deficiency but focuses on the resultant disease state. The only...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awdur: Sandhaus, R
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BMJ Group 2004
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC1746849/
https://ncbi.nlm.nih.gov/pubmed/15454659
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/thx.2003.006551
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