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HARVARD Citation
Labrouche-Colomer, S. et al. (2020). A novel rare c.-39C>T mutation in the PROS1 5′UTR causing PS deficiency by creating a new upstream translation initiation codone. Clinical science. 134 (10), pp. 1181-1190. [Online].
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Labrouche-Colomer, S. et al. (2020). A novel rare c.-39C>T mutation in the PROS1 5′UTR causing PS deficiency by creating a new upstream translation initiation codone. Clinical science. 134 (10), pp. 1181-1190. [Online].