TY  - GEN 
AU  - Vázquez-Román, V.
AU  - Cameselle Teijeiro, Jose Manuel
AU  - Fernández-Santos, J.M.
AU  - Ríos-Moreno, M.J.
AU  - Loidi Fernández de Trocóniz, Lourdes
AU  - Ortiz, T.
AU  - Martín-Lacave, I.
PY  - 2022
SN  - 1559-0097
UR  - http://hdl.handle.net/20.500.11940/20932
AB  - Pendred syndrome (PDS) is an autosomal recessive disorder caused by mutations in the gene that encodes pendrin. Pendred thyroid tissue is supposedly altered by the absence of functional pendrin, but it is still unknown whether other iodide exchangers...
LA  - eng
TI  - Histopathological Features of Pendred Syndrome Thyroids Align with Differences in the Expression of Thyroid-Specific Markers, Apical Iodide Transporters, and Ciliogenesis Process
DO  - 10.1007/s12022-022-09732-2
KW  - IDIS
KW  - AS Santiago
KW  - CHUS
KW  - FPGMX
VL  - 33
ER  -