Free Access
Med Sci (Paris)
Volume 28, Number 4, Avril 2012
Page(s) 435 - 437
Section Forum
Published online 25 April 2012
  1. Katsnelson A. Breaking the silence. Nat Med 2011 ; 17 : 1536–1538. [CrossRef] [PubMed] [Google Scholar]
  2. Kimchi-Sarfaty C, Oh JM, Kim IW, et al. A « silent » polymorphism in the MDR1 gene changes substrate specificity. Science 2007 ; 315 : 525–528. [CrossRef] [PubMed] [Google Scholar]
  3. Nackley AG, Shabalina SA, Tchivileva IE, et al. Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure. Science 2006 ; 314 : 1930–1933. [CrossRef] [PubMed] [Google Scholar]
  4. Chen R, Davydov EV, Sirota M, Butte AJ. Non-synonymous and synonymous coding SNPs show similar likelihood and effect size of human disease association. PLoS One 2010 ; 5 : e13574. [CrossRef] [PubMed] [Google Scholar]
  5. International HapMap Consortium, Frazer KA, Ballinger DG, Cox DR, et al. A second generation human haplotype map of over 3.1 million SNPs. Nature 2007 ; 449 : 851–861. [CrossRef] [PubMed] [Google Scholar]
  6. Sauna ZE, Kimchi-Sarfaty C. Understanding the contribution of synonymous mutations to human disease. Nat Rev Genet 2011 ; 12 : 683–691. [CrossRef] [PubMed] [Google Scholar]
  7. Sempé JJ. Rien n’est simple. Paris : Denoël 1962. [Google Scholar]

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