Associated Papers
Consequences of the 118A>G polymorphism in the OPRM1 gene: translation from bench to bedside?
Mura E et al.
Journal of Pain Research, 2013
Identification of mutations in 90 of 121 consecutive symptomatic French patients with a type I protein C deficiency. The French INSERM Network on Molecular Abnormalities Responsible for Protein C and Protein S deficiencies.
Gandrille S et al.
Blood, 1995
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