Whole exome sequencing in multi-incident families identifies novel candidate genes for multiple sclerosis

HIGHLIGHTS

• who: Julia Horjus and collaborators from the Department of Human Genetics, Radboud University Medical Center, HB Nijmegen, The Netherlands have published the paper: Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis, in the Journal: (JOURNAL) of 28/02/2022
• what: While most genetic studies have focused on identifying common genetic variants for MS through genome-wide association studies the objective of this study was to identify rare genetic variants contributing to MS susceptibility. The approach provides clues to possible molecular mechanisms underlying MS that should be studied further in . . .
  

   

  

  If you want to have access to all the content you need to log in!

  Thanks :)

  Username or E-mail:

  If you don't have an account, you can create one here.