An unusual case of alpha-1-antitrypsin deficiency: SZ/Z.

We report the investigations used to clarify her unusual genotype and propose non-crossover gene conversion as the likely mechanism.
PMID: 30579752 [PubMed - as supplied by publisher]

Source: Clinical Biochemistry - December 20, 2018 Category: Biochemistry Authors: Speevak MD, DeMarco ML, Wiebe NS, Chapman KR Tags: Clin Biochem Source Type: research