Associated Papers
Monocarboxylate Transporter 8 Deficiency: Delayed or Permanent Hypomyelination?
Vancamp P et al.
Frontiers in Endocrinology, 2020
Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency.
Masnada S et al.
Metabolic Brain Disease, 2019
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