| 000 | 01739 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250516140720.0 | ||
| 264 | 0 | _c20131112 | |
| 008 | 201311s 0 0 eng d | ||
| 022 | _a1096-7206 | ||
| 024 | 7 |
_a10.1016/j.ymgme.2013.01.017 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBrassier, Anaïs | |
| 245 | 0 | 0 |
_aDihydrolipoamide dehydrogenase deficiency: a still overlooked cause of recurrent acute liver failure and Reye-like syndrome. _h[electronic resource] |
| 260 |
_bMolecular genetics and metabolism _cMay 2013 |
||
| 300 |
_a28-32 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAcidosis, Lactic _xblood |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAlgeria |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 |
_aDihydrolipoamide Dehydrogenase _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aLiver _xpathology |
| 650 | 0 | 4 |
_aLiver Failure, Acute _xblood |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMaple Syrup Urine Disease _xblood |
| 650 | 0 | 4 |
_aMuscles _xpathology |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aReye Syndrome _xgenetics |
| 700 | 1 | _aOttolenghi, Chris | |
| 700 | 1 | _aBoutron, Audrey | |
| 700 | 1 | _aBertrand, Anne-Marie | |
| 700 | 1 | _aValmary-Degano, Séverine | |
| 700 | 1 | _aCervoni, Jean-Paul | |
| 700 | 1 | _aChrétien, Dominique | |
| 700 | 1 | _aArnoux, Jean-Baptiste | |
| 700 | 1 | _aHubert, Laurence | |
| 700 | 1 | _aRabier, Daniel | |
| 700 | 1 | _aLacaille, Florence | |
| 700 | 1 | _ade Keyzer, Yves | |
| 700 | 1 | _aDi Martino, Vincent | |
| 700 | 1 | _ade Lonlay, Pascale | |
| 773 | 0 |
_tMolecular genetics and metabolism _gvol. 109 _gno. 1 _gp. 28-32 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ymgme.2013.01.017 _zAvailable from publisher's website |
| 999 |
_c22570066 _d22570066 |
||