| 000 | 01819 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250514192237.0 | ||
| 264 | 0 | _c20050217 | |
| 008 | 200502s 0 0 eng d | ||
| 022 | _a0946-2716 | ||
| 024 | 7 |
_a10.1007/s00109-004-0557-9 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aStuehler, Bettina | |
| 245 | 0 | 0 |
_aAnalysis of the human homologue of the canine copper toxicosis gene MURR1 in Wilson disease patients. _h[electronic resource] |
| 260 |
_bJournal of molecular medicine (Berlin, Germany) _cSep 2004 |
||
| 300 |
_a629-34 p. _bdigital |
||
| 500 | _aPublication Type: Comparative Study; Journal Article | ||
| 650 | 0 | 4 | _aAdaptor Proteins, Signal Transducing |
| 650 | 0 | 4 |
_aAdenosine Triphosphatases _xgenetics |
| 650 | 0 | 4 | _aAge of Onset |
| 650 | 0 | 4 | _aAmino Acid Substitution |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 | _aCarrier Proteins |
| 650 | 0 | 4 |
_aCation Transport Proteins _xgenetics |
| 650 | 0 | 4 |
_aCodon _xgenetics |
| 650 | 0 | 4 |
_aCopper _xmetabolism |
| 650 | 0 | 4 | _aCopper-Transporting ATPases |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 |
_aDog Diseases _xgenetics |
| 650 | 0 | 4 | _aDogs |
| 650 | 0 | 4 |
_aExons _xgenetics |
| 650 | 0 | 4 | _aGenetic Heterogeneity |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 |
_aHepatolenticular Degeneration _xepidemiology |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntrons _xgenetics |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 | _aPolymorphism, Genetic |
| 650 | 0 | 4 |
_aProteins _xgenetics |
| 650 | 0 | 4 | _aSpecies Specificity |
| 700 | 1 | _aReichert, Juergen | |
| 700 | 1 | _aStremmel, Wolfgang | |
| 700 | 1 | _aSchaefer, Mark | |
| 773 | 0 |
_tJournal of molecular medicine (Berlin, Germany) _gvol. 82 _gno. 9 _gp. 629-34 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s00109-004-0557-9 _zAvailable from publisher's website |
| 999 |
_c14911351 _d14911351 |
||