Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes

Lignende værker

• Assessing the functional consequence of loss of function variants using electronic medical record and large-scale genomics consortium efforts
  af: Sleiman, Patrick, et al.
  Udgivet: (2014)
• Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts
  af: Connolly, John J., et al.
  Udgivet: (2014)
• Mendelian randomization analysis demonstrates that low vitamin D is unlikely causative for pediatric asthma
  af: Hysinger, Erik B., et al.
  Udgivet: (2016)
• Genetic Underpinnings of Obstructive Sleep Apnea: Are We Making Progress?
  af: Sleiman, Patrick, et al.
  Udgivet: (2011)
• Enhanced proteolysis of thiopurine S-methyltransferase (TPMT) encoded by mutant alleles in humans (TPMT∗3A, TPMT∗2): Mechanisms for the genetic polymorphism of TPMT activity
  af: Tai, Hung-Liang, et al.
  Udgivet: (1997)