A Novel Rare c.-39C>T Mutation in the PROS1 5'UTR Causing PS Deficiency by Creating a New Upstream Translation Initiation Codons.
Labrouche-Colomer S, Soukarieh O, Proust C, Mouton C, Huguenin Y, Roux M , Besse C, Boland A, Olaso R , Constans J, Deleuze JF , Morange PE , Jaspard-Vinassa B , Trégouët DA.
Clin Sci (Lond) 2020 May 19;CS20200403. doi: 10.1042/CS20200403. Online ahead of print [PMID: 32426810].