Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

Gelijkaardige items

• Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
  door: O'Roak, B, et al.
  Gepubliceerd in: (2011)
• Mutations and modeling of the chromatin remodeler CHD8 define an emerging autism etiology
  door: Rebecca A Barnard, et al.
  Gepubliceerd in: (2015-12-01)
• Exome sequencing reveals a de novo PRKG1 mutation in a sporadic patient with aortic dissection
  door: Wenwen Zhang, et al.
  Gepubliceerd in: (2018-12-01)
• Whole-exome sequencing of 228 patients with sporadic Parkinson's disease.
  door: Sandor, C, et al.
  Gepubliceerd in: (2017)
• Whole-exome sequencing studies of nonhereditary (sporadic) parathyroid adenomas.
  door: Newey, P, et al.
  Gepubliceerd in: (2012)