Defining the clinical risks associated with CPT1a p.P479L homozygosity in children from BC First Nations

Project number: 
Approval date: 
Monday, October 28, 2013
Principal Investigator: 
BC Childrens Hospital
Funding Agency: 
BC Childrens Hospital Telethon Competition
Datasets requested: 
Not available
Research objective: 

Journal Publication

  • Sinclair G, Collins S,
    Arbour L, Vallance H. The p.P479L variant in CPT1A is associated with
    infectious disease in a BC First Nation. Paediatrics and Child Health. ePub
    ahead of print Aug 2018. Available at:

Page last revised: September 2, 2019