| 000 | 01726 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250514064454.0 | ||
| 264 | 0 | _c20030527 | |
| 008 | 200305s 0 0 eng d | ||
| 022 | _a1061-4036 | ||
| 024 | 7 |
_a10.1038/ng1147 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aCarlton, Victoria E H | |
| 245 | 0 | 0 |
_aComplex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT. _h[electronic resource] |
| 260 |
_bNature genetics _cMay 2003 |
||
| 300 |
_a91-6 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 |
_aAcyltransferases _xgenetics |
| 650 | 0 | 4 |
_aBile Acids and Salts _xblood |
| 650 | 0 | 4 | _aCase-Control Studies |
| 650 | 0 | 4 |
_aEthnicity _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aLinkage Disequilibrium |
| 650 | 0 | 4 |
_aLiver _xpathology |
| 650 | 0 | 4 |
_aMalabsorption Syndromes _xblood |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMembrane Proteins _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPennsylvania |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aTight Junctions _xpathology |
| 650 | 0 | 4 | _aZonula Occludens-2 Protein |
| 700 | 1 | _aHarris, Baruch Z | |
| 700 | 1 | _aPuffenberger, Erik G | |
| 700 | 1 | _aBatta, A K | |
| 700 | 1 | _aKnisely, A S | |
| 700 | 1 | _aRobinson, Donna L | |
| 700 | 1 | _aStrauss, Kevin A | |
| 700 | 1 | _aShneider, Benjamin L | |
| 700 | 1 | _aLim, Wendell A | |
| 700 | 1 | _aSalen, Gerald | |
| 700 | 1 | _aMorton, D Holmes | |
| 700 | 1 | _aBull, Laura N | |
| 773 | 0 |
_tNature genetics _gvol. 34 _gno. 1 _gp. 91-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1038/ng1147 _zAvailable from publisher's website |
| 999 |
_c12495881 _d12495881 |
||