HuGE Literature Finder
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| Association of the CPT1A p.P479L Metabolic Gene Variant With Childhood Respiratory and Other Infectious Illness in Nunavut. Frontiers in pediatrics 2021 7 9 678553. Collins Sorcha A, Edmunds Sharon, Akearok Gwen Healey, Thompson J Robert, Erickson Anders C, Hildes-Ripstein Elske, Miners Amber, Somerville Martin, Goldfarb David M, Rockman-Greenberg Cheryl, Arbour Lau |
| The p.P479L variant in CPT1A is associated with infectious disease in a BC First Nation. Paediatrics & child health 2019 4 24 (2): e111-e115. Sinclair Graham, Collins Sorcha, Arbour Laura, Vallance Hila |
| Carnitine palmitoyltransferase I and sudden unexpected infant death in British Columbia First Nations. Pediatrics 2012 Oct . Sinclair GB, Collins S, Popescu O, McFadden D, Arbour L, Vallance HD |
| Evidence for an association between infant mortality and a carnitine palmitoyltransferase 1A genetic variant. Pediatrics 2010 Nov 126 (5): 945-51. Gessner Bradford D, Gillingham Melanie B, Birch Stephanie, Wood Thalia, Koeller David |
| Carnitine palmitoyltransferase 1A (CPT1A) P479L prevalence in live newborns in Yukon, Northwest Territories, and Nunavut. Molecular genetics and metabolism 0 101 (2-3): 200-4. Collins Sorcha A, Sinclair Graham, McIntosh Sarah, Bamforth Fiona, Thompson Robert, Sobol Isaac, Osborne Geraldine, Corriveau Andre, Santos Maria, Hanley Brendan, Greenberg Cheryl R, Vallance Hilary, Arbour Lau |
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