| 000 | 01887 a2200577 4500 | ||
|---|---|---|---|
| 005 | 20250515224914.0 | ||
| 264 | 0 | _c20140408 | |
| 008 | 201404s 0 0 eng d | ||
| 022 | _a1573-2665 | ||
| 024 | 7 |
_a10.1007/s10545-010-9123-5 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aWeiss, Karl Heinz | |
| 245 | 0 | 0 |
_aGenetic analysis of BIRC4/XIAP as a putative modifier gene of Wilson disease. _h[electronic resource] |
| 260 |
_bJournal of inherited metabolic disease _cDec 2010 |
||
| 300 |
_aS233-40 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAdenosine Triphosphatases _xgenetics |
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAge of Onset |
| 650 | 0 | 4 |
_aCation Transport Proteins _xgenetics |
| 650 | 0 | 4 | _aChi-Square Distribution |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aCopper-Transporting ATPases |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGene Frequency |
| 650 | 0 | 4 | _aGenes, Modifier |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 |
_aHepatolenticular Degeneration _xdiagnosis |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aRisk Factors |
| 650 | 0 | 4 |
_aX-Linked Inhibitor of Apoptosis Protein _xgenetics |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aRunz, Heiko | |
| 700 | 1 | _aNoe, Barbara | |
| 700 | 1 | _aGotthardt, Daniel Nils | |
| 700 | 1 | _aMerle, Uta | |
| 700 | 1 | _aFerenci, Peter | |
| 700 | 1 | _aStremmel, Wolfgang | |
| 700 | 1 | _aFüllekrug, Joachim | |
| 773 | 0 |
_tJournal of inherited metabolic disease _gvol. 33 Suppl 3 _gp. S233-40 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s10545-010-9123-5 _zAvailable from publisher's website |
| 999 |
_c19869002 _d19869002 |
||