| 000 | 01898 a2200577 4500 | ||
|---|---|---|---|
| 005 | 20250515064716.0 | ||
| 264 | 0 | _c20070815 | |
| 008 | 200708s 0 0 eng d | ||
| 022 | _a0888-8809 | ||
| 024 | 7 |
_a10.1210/me.2007-0040 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSasaki, Nobuya | |
| 245 | 0 | 0 |
_aA mutation in Tpst2 encoding tyrosylprotein sulfotransferase causes dwarfism associated with hypothyroidism. _h[electronic resource] |
| 260 |
_bMolecular endocrinology (Baltimore, Md.) _cJul 2007 |
||
| 300 |
_a1713-21 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAmino Acid Sequence |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 |
_aCongenital Hypothyroidism _xcomplications |
| 650 | 0 | 4 |
_aDNA Primers _xgenetics |
| 650 | 0 | 4 |
_aDwarfism _xcomplications |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Complementation Test |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMice |
| 650 | 0 | 4 | _aMice, Inbred C57BL |
| 650 | 0 | 4 | _aMice, Mutant Strains |
| 650 | 0 | 4 | _aMice, Transgenic |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aProtein Processing, Post-Translational |
| 650 | 0 | 4 |
_aReceptors, Thyrotropin _xmetabolism |
| 650 | 0 | 4 | _aSequence Homology, Amino Acid |
| 650 | 0 | 4 | _aSignal Transduction |
| 650 | 0 | 4 | _aSubstrate Specificity |
| 650 | 0 | 4 |
_aSulfotransferases _xdeficiency |
| 650 | 0 | 4 |
_aThyrotropin _xmetabolism |
| 700 | 1 | _aHosoda, Yayoi | |
| 700 | 1 | _aNagata, Aogu | |
| 700 | 1 | _aDing, Ming | |
| 700 | 1 | _aCheng, Ji-Ming | |
| 700 | 1 | _aMiyamoto, Tomomi | |
| 700 | 1 | _aOkano, Shinya | |
| 700 | 1 | _aAsano, Atsushi | |
| 700 | 1 | _aMiyoshi, Ichiro | |
| 700 | 1 | _aAgui, Takashi | |
| 773 | 0 |
_tMolecular endocrinology (Baltimore, Md.) _gvol. 21 _gno. 7 _gp. 1713-21 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1210/me.2007-0040 _zAvailable from publisher's website |
| 999 |
_c17006059 _d17006059 |
||