TY  - JOUR
AU  - Grijota Martínez, María Carmen
AU  - Bárez López, Soledad
AU  - Ausó, Eva
AU  - Refetoff, Samuel
AU  - Frey, William H.
AU  - Guadaño Ferraz, Ana
AU  - Iglesias Osma, Maria Carmen
PY  - 2020
DO  - 10.1371/journal.pone.0236113
SN  - 1932-6203
UR  - https://hdl.handle.net/20.500.14352/92644
T2  - PLoS ONE
AB  - Loss of function mutations in the gene encoding the thyroid hormone transporter monocarboxylate transporter 8 (MCT8) lead to severe neurodevelopmental defects in humans associated with a specific thyroid hormone phenotype manifesting high serum...
LA  - eng
M2  - 1
PB  - Public Library of Science
TI  - Intranasal delivery of thyroid hormones in MCT8 deficiency
TY  - journal article
VL  - 15
ER  -