A novel heterozygous frameshift c.277del p.Thr93Leufs*21 mutation in SERPINC1 associated with type 1 antithrombin deficiency.

Autor: Kumar, Riten, Duzan, Juliann, Drake, Emily, Dawson, Jennifer
Zdroj: Pediatric Blood & Cancer; Jun2024, Vol. 71 Issue 6, p1-3, 3p
Databáze: Complementary Index
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