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A novel rare c.-39C > T mutation in the PROS1 5 ' UTR causing PS deficiency by creating a new upstream translation initiation codone

Published on 2 October 2023
A novel rare c.-39C > T mutation in the PROS1 5 ' UTR causing PS deficiency by creating a new upstream translation initiation codone
Description
 
Date de publication 
Auteurs
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, Tregouet DA and GenMed C
Revue
Année2,020
Département / Service
CNRGH
Laboratoire
LBanq, LHD
Impact Factor 
InstitutJACOB
url DOI10.1042/cs20200403

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