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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MSU College of Osteopathic Medicine Statewide Campus System
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746044/ https://www.ncbi.nlm.nih.gov/pubmed/33655122 http://dx.doi.org/10.51894/001c.6382 |