Monocarboxylate Transporter 8 Deficiency: Delayed or Permanent Hypomyelination?

Monocarboxylate Transporter 8 Deficiency: Delayed or Permanent Hypomyelination?

Monocarboxylate transporter 8 (MCT8) deficiency or the Allan-Herndon-Dudley Syndrome (AHDS) is an X-linked psychomotor disability syndrome with around 320 clinical cases described worldwide. SLC16A2 gene mutations, encoding the thyroid hormone (TH) transporter MCT8, result in intellectual disability...

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Bibliographic Details
Main Authors: Pieter Vancamp, Barbara A. Demeneix, Sylvie Remaud
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-05-01
Series:Frontiers in Endocrinology
Subjects:
Allan-Herndon-Dudley Syndrome
SLC16A2 gene
monocarboxylate transporter 8
oligodendrocyte
myelination and myelin repair
thyroid hormones
Online Access:https://www.frontiersin.org/article/10.3389/fendo.2020.00283/full

Internet

https://www.frontiersin.org/article/10.3389/fendo.2020.00283/full

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