Investigating the pathogenic impact of mutations in C21 or F60 as the genetic cause of a novel developmental disorder in children

Project Details

Short titleInvestigating the pathogenic impact of mutations in C21 or F60 as the genetic cause of a novel developmental disorder in children
StatusFinished
Effective start/end date4/01/16 → 3/01/20

Funding

  • BIRMINGHAM CHILDRENS HOSPITAL RESEARCH FOUNDATION