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Updated: Jun 29, 2025

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Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
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A novel heterozygous frameshift c.277del p.Thr93Leufs*21 mutation in SERPINC1 associated with type 1 antithrombin
Riten Kumar1,2, Juliann Duzan1, Emily Drake1
1Dana Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts, USA.
Pediatric Blood & Cancer
|April 2, 2024
Abstract
No abstract available in PubMed .
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