| 000 | 01770 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250516044836.0 | ||
| 264 | 0 | _c20120119 | |
| 008 | 201201s 0 0 eng d | ||
| 022 | _a1873-2364 | ||
| 024 | 7 |
_a10.1016/j.nmd.2011.04.013 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aNouioua, Sonia | |
| 245 | 0 | 0 |
_aNovel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes. _h[electronic resource] |
| 260 |
_bNeuromuscular disorders : NMD _cAug 2011 |
||
| 300 |
_a543-50 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAlgeria |
| 650 | 0 | 4 |
_aCharcot-Marie-Tooth Disease _xethnology |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIncidence |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMembrane Proteins _xgenetics |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aProtein Tyrosine Phosphatases, Non-Receptor _xgenetics |
| 650 | 0 | 4 | _aRetrospective Studies |
| 650 | 0 | 4 |
_aScoliosis _xepidemiology |
| 650 | 0 | 4 |
_aThorax _xabnormalities |
| 650 | 0 | 4 |
_aVocal Cord Paralysis _xepidemiology |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aHamadouche, Tarik | |
| 700 | 1 | _aFunalot, Benoit | |
| 700 | 1 | _aBernard, Rafaëlle | |
| 700 | 1 | _aBellatache, Nora | |
| 700 | 1 | _aBouderba, Radia | |
| 700 | 1 | _aGrid, Djamel | |
| 700 | 1 | _aAssami, Salima | |
| 700 | 1 | _aBenhassine, Traki | |
| 700 | 1 | _aLevy, Nicolas | |
| 700 | 1 | _aVallat, Jean-Michel | |
| 700 | 1 | _aTazir, Meriem | |
| 773 | 0 |
_tNeuromuscular disorders : NMD _gvol. 21 _gno. 8 _gp. 543-50 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.nmd.2011.04.013 _zAvailable from publisher's website |
| 999 |
_c20993357 _d20993357 |
||