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The New England Journal of Medicine, ISSN 0028-4793, 06/2016, Volume 374, Issue 23, pp. 2246 - 2255
Journal Article
Paediatrics & Child Health, ISSN 1205-7088, 04/2019, Volume 24, Issue 2, pp. e111 - e115
Abstract Background The hepatic carnitine palmitoyltransferase I (CPT1A) p.P479L variant is common in Aboriginal populations across coastal British Columbia,... 
Fatty acid oxidation | Infection | Indigenous | Carnitine palmitoyltransferase | First Nation | Carnitine palmitoyltransferase deficiency | Care and treatment | Hospital care | Canadian native peoples | Genetic aspects | Children | Observations | Health aspects | Diseases
Journal Article
The Journal of nutrition, ISSN 0022-3166, 08/2019, Volume 149, Issue 12, pp. 2145 - 2155
As a methyl donor required in the folate-vitamin B-12 independent remethylation of total homocysteine (tHcy) to methionine, betaine is critical for fetal... 
Journal Article
Science, ISSN 0036-8075, 10/2010, Volume 330, Issue 6002, pp. 336 - 336
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 03/2014, Volume 94, Issue 3, pp. 453 - 461
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 10/2015, Volume 23, Issue 10, pp. 1301 - 1307
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 03/2019, Volume 14, Issue 1, pp. 70 - 10
Journal Article
Clinical Biochemistry, ISSN 0009-9120, 10/2014, Volume 47, Issue 15, pp. 145 - 145
Journal Article