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Update on α(1)-antitrypsin deficiency
α(1)-Antitrypsin deficiency (AATD) is an inherited metabolic disorder in which mutations in the coding sequence of the SERPINA1 gene prevent secretion of α(1)-antitrypsin (α(1)-AT) and cause predisposition to pulmonary and liver diseases. The heterogeneity of clinical manifestations in AATD is relat...
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| Publicado no: | Breathe (Sheff) |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
European Respiratory Society
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6095240/ https://ncbi.nlm.nih.gov/pubmed/30131830 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1183/20734735.015018 |
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