TY  - JOUR
AU  - Grijota Martínez, María Carmen
AU  - Díez, Diego
AU  - Morreale de Escobar, Gabriella
AU  - Bernal, Juan
AU  - Morte, Beatriz
PY  - 2011
DO  - 10.1210/en.2010-1014
SN  - 0013-7227
UR  - https://hdl.handle.net/20.500.14352/92381
T2  - Endocrinology
AB  - Mutations of the monocarboxylate transporter 8 gene (MCT8, SLC16A2) cause the Allan-Herndon-Dudley syndrome, an X-linked syndrome of severe intellectual deficit and neurological impairment. Mct8 transports thyroid hormones (T4 and T3), and the...
LA  - eng
M2  - 1713
PB  - Oxford University Press
TI  - Lack of action of exogenously administered T3 on the fetal rat brain despite expression of the monocarboxylate transporter 8
TY  - journal article
VL  - 152
ER  -