Nalaganje...
MCT8 Deficiency: The Road to Therapies for a Rare Disease
Allan-Herndon-Dudley syndrome is a rare disease caused by inactivating mutations in the SLC16A2 gene, which encodes the monocarboxylate transporter 8 (MCT8), a transmembrane transporter specific for thyroid hormones (T3 and T4). Lack of MCT8 function produces serious neurological disturbances, most...
Shranjeno v:
| izdano v: | Front Neurosci |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Frontiers Media S.A.
2020
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7198743/ https://ncbi.nlm.nih.gov/pubmed/32410949 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2020.00380 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|