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

Project number: 
13-054
Approval date: 
Monday, October 28, 2013
Principal Investigator: 
Sinclair,Graham
Institution: 
BC Childrens Hospital
Funding Agency: 
BC Childrens Hospital Telethon Competition
Datasets requested: 
Not available
Research objective: 
Publications: 

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: https://doi.org/10.1093/pch/pxy106

Page last revised: September 2, 2019