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SLC16A2 protein
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Curated Studies
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Brain microvascular endothelial cells and neural cells from iPSC of MCT8-deficient patients
Effects of monocarboxylate transporter 8 (MCT8) mutation on skin fibroblast gene expression
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A novel variant in SLC16A2 associated with typical Allan-Herndon-Dudley syndrome: a case report.
Delayed Myelination Pattern and an Abnormal Thyroid Profile Caused by a Novel Mutation in the SLC16A…
Chromosomal microarray and exome sequencing in unexplained early infantile epileptic encephalopathie…
Repetitive Sleep Starts in Allan-Herndon-Dudley Syndrome.
Maternal Exercise Before and During Pregnancy Facilitates Embryonic Myogenesis by Enhancing Thyroid …
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Glycerol-Phenylbutyrate Treatment in Children With MCT Mutation (Allan-Herndon- Dudley Syndrome)
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