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

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

Pediatr Blood Cancer. 2024 Apr 2:e30986. doi: 10.1002/pbc.30986. Online ahead of print.

NO ABSTRACT

PMID:38563157 | DOI:10.1002/pbc.30986