TY  - JOUR
AU  - López Espíndola, Daniela
AU  - Morales Bastos, Carmen
AU  - Grijota Martínez, María Carmen
AU  - Liao, Xiao-Hui
AU  - Lev, Dorit
AU  - Sugo, Ella
AU  - Verge, Charles F.
AU  - Refetoff, Samuel
AU  - Bernal, Juan
AU  - Guadaño Ferraz, Ana
PY  - 2014
DO  - 10.1210/jc.2014-2162
SN  - 0021-972X
UR  - https://hdl.handle.net/20.500.14352/92576
T2  - The Journal of Clinical Endocrinology & Metabolism
AB  - Context: Mutations in the MCT8 (SLC16A2) gene, encoding a specific thyroid hormone transporter, cause an X-linked disease with profound psychomotor retardation, neurological impairment, and abnormal serum thyroid hormone levels. The nature of the...
LA  - eng
M2  - 2799
PB  - Oxford University Press
TI  - Mutations of the thyroid hormone transporter MCT8 cause prenatal brain bamage and persistent hypomyelination
TY  - journal article
VL  - 99
ER  -