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ArticleChronic obstructive pulmonary diseases (Miami, Fla.)2021

The Clinical Utility of Determining the Allelic Background of Mutations Causing Alpha-1 Antitrypsin Deficiency: The Case with the Null Variant Q0(Mattawa)/Q0(Ourém).

Judith Bellemare et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2021
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Full record →Abstract, authors, funding and every citing paper · PMID 33150777