Associated Papers
Mitochondrial bioenergetic is impaired in Monocarboxylate transporter 1 deficiency: a new clinical case and review of the literature.
Stanescu S et al.
Orphanet Journal of Rare Diseases, 2022
Heterozygous Monocarboxylate Transporter 1 (MCT1, SLC16A1) Deficiency as a Cause of Recurrent Ketoacidosis.
Balasubramaniam S et al.
Jimd Reports, 2016
Monocarboxylate transporter 1 deficiency and ketone utilization.
van Hasselt PM et al.
The New England Journal of Medicine, 2014
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