Unmet patient needs in monocarboxylate transporter 8 (MCT8) deficiency: a review

Unmet patient needs in monocarboxylate transporter 8 (MCT8) deficiency: a review

Monocarboxylate transporter 8 (MCT8) deficiency is a rare, X-linked disorder arising from mutations in the SLC16A2 gene and resulting from dysfunctional thyroid hormone transport. This disorder is characterized by profound neurodevelopmental delay and motor disability due to a lack of thyroid hormon...

Full description

Saved in:
Bibliographic Details
Main Authors: Andrew J. Bauer (Author), Bethany Auble (Author), Amy L. Clark (Author), Tina Y. Hu (Author), Amber Isaza (Author), Kyle P. McNerney (Author), Daniel L. Metzger (Author), Lindsey Nicol (Author), Samuel R. Pierce (Author), Richard Sidlow (Author)
Format: Book
Published: Frontiers Media S.A., 2024-07-01T00:00:00Z.
Subjects:
article
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available

Similar Items