000 01555 a2200409 4500
005 20250514030450.0
264 0 _c20020425
008 200204s 0 0 eng d
022 _a0021-972X
024 7 _a10.1210/jcem.87.4.8435
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aTaylor, Julie P
245 0 0 _aMutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome.
_h[electronic resource]
260 _bThe Journal of clinical endocrinology and metabolism
_cApr 2002
300 _a1778-84 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aBiological Transport
_xgenetics
650 0 4 _aCarrier Proteins
_xgenetics
650 0 4 _aCell Line
650 0 4 _aGoiter
_xgenetics
650 0 4 _aHeLa Cells
650 0 4 _aHearing Loss, Sensorineural
_xgenetics
650 0 4 _aHumans
650 0 4 _aIodides
_xmetabolism
650 0 4 _aMembrane Transport Proteins
650 0 4 _aMutation
_xphysiology
650 0 4 _aSulfate Transporters
650 0 4 _aSyndrome
650 0 4 _aThyroid Gland
_xphysiopathology
650 0 4 _aTissue Distribution
700 1 _aMetcalfe, Russell A
700 1 _aWatson, Philip F
700 1 _aWeetman, Anthony P
700 1 _aTrembath, Richard C
773 0 _tThe Journal of clinical endocrinology and metabolism
_gvol. 87
_gno. 4
_gp. 1778-84
856 4 0 _uhttps://doi.org/10.1210/jcem.87.4.8435
_zAvailable from publisher's website
999 _c11836567
_d11836567