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 |