Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease

Eitemau Tebyg

• Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
  gan: Raghavan, Neha S., et al.
  Cyhoeddwyd: (2018)
• Whole-Exome Sequencing for the Discovery of Rare Genetic Variants That Protect from Coronary Artery Disease
  gan: Leopold, Jane A.
  Cyhoeddwyd: (2016)
• Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease
  gan: Desch, Karl C., et al.
  Cyhoeddwyd: (2020)
• Clinical Utility of Whole-Exome Sequencing in Rare Diseases: Galactosialidosis
  gan: Prada, Carlos E., et al.
  Cyhoeddwyd: (2014)
• Identification of rare paired box 3 variant in strabismus by whole exome sequencing
  gan: Gong, Hui-Min, et al.
  Cyhoeddwyd: (2017)