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Alpha 1 Antitrypsin Deficiency, Two Cases of Heterozygous S and Clayton Null Alleles
Alpha-1 antitrypsin deficiency (AATD) is a disorder that can lead to early onset lung and liver disease and is considered to be underdiagnosed. The purpose of this paper is to demonstrate the importance of early detection using genotyping of AATD by presenting two very rare cases of this disorder an...
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| Publicat a: | Spartan Med Res J |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MSU College of Osteopathic Medicine Statewide Campus System
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7746044/ https://ncbi.nlm.nih.gov/pubmed/33655122 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.51894/001c.6382 |
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