Hereditary of Alpha-1-Antitrypsin Deficiency
| Author | Sara Gholami | en |
| Author | Tayebeh Hamzehloei | en |
| Orcid | Tayebeh Hamzehloei [0000-0002-5510-3387] | en |
| Issued Date | 2013-03-01 | en |
| Abstract | In this review article, in addition to the clinical manifestation of the alpha 1 antitrypsin deficiency, the genetics and molecular diagnosis of the disease and the effects of the causative mutations were reviewed. | en |
| DOI | https://doi.org/ | en |
| Keyword | Alpha 1 antitrypsin deficiency | en |
| Keyword | Pi ZZ | en |
| Keyword | Molecular diagnosis of AATD | en |
| Publisher | Brieflands | en |
| Title | Hereditary of Alpha-1-Antitrypsin Deficiency | en |
| Type | Review Article | en |
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