TY  - JOUR
AU  - Grijota Martínez, María Carmen
AU  - Bárez López, Soledad
AU  - Gómez Andrés, David
AU  - Guadaño Ferraz, Ana
AU  - Granata, Riccarda
PY  - 2020
DO  - 10.3389/fnins.2020.00380
SN  - 1662-453X
UR  - https://hdl.handle.net/20.500.14352/92620
T2  - Frontiers in Neuroscience
AB  - 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...
LA  - eng
M2  - 1
PB  - Frontiers 
KW  - Thyroid hormones
KW  - Brain
KW  - Neurodevelopment
KW  - MCT8
KW  - DITPA
KW  - Sobetirome
KW  - TRIAC
TI  - MCT8 Deficiency: The Road to therapies for a Rare Disease
TY  - journal article
VL  - 14
ER  -