TY  - GEN
AU  - Taylor,Julie P
AU  - Metcalfe,Russell A
AU  - Watson,Philip F
AU  - Weetman,Anthony P
AU  - Trembath,Richard C
TI  - Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome
SN  - 0021-972X
PY  - 2002///0425
KW  - Biological Transport
KW  - genetics
KW  - Carrier Proteins
KW  - Cell Line
KW  - Goiter
KW  - HeLa Cells
KW  - Hearing Loss, Sensorineural
KW  - Humans
KW  - Iodides
KW  - metabolism
KW  - Membrane Transport Proteins
KW  - Mutation
KW  - physiology
KW  - Sulfate Transporters
KW  - Syndrome
KW  - Thyroid Gland
KW  - physiopathology
KW  - Tissue Distribution
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1210/jcem.87.4.8435
ER  -