| 000 | 01593 a2200481 4500 | ||
|---|---|---|---|
| 005 | 20250517095848.0 | ||
| 264 | 0 | _c20170411 | |
| 008 | 201704s 0 0 eng d | ||
| 022 | _a1432-1459 | ||
| 024 | 7 |
_a10.1007/s00415-016-8167-3 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aRenaud, Mathilde | |
| 245 | 0 | 0 |
_aExpanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia. _h[electronic resource] |
| 260 |
_bJournal of neurology _cAug 2016 |
||
| 300 |
_a1552-8 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 |
_aBrain _xdiagnostic imaging |
| 650 | 0 | 4 |
_aCerebellar Ataxia _xgenetics |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aDisability Evaluation |
| 650 | 0 | 4 | _aDisease Progression |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 |
_aMutation, Missense _xgenetics |
| 650 | 0 | 4 | _aPeroxins |
| 650 | 0 | 4 |
_aPeroxisomal Disorders _xblood |
| 650 | 0 | 4 |
_aReceptors, Cytoplasmic and Nuclear _xgenetics |
| 700 | 1 | _aGuissart, Claire | |
| 700 | 1 | _aMallaret, Martial | |
| 700 | 1 | _aFerdinandusse, Sacha | |
| 700 | 1 | _aCheillan, David | |
| 700 | 1 | _aDrouot, Nathalie | |
| 700 | 1 | _aMuller, Jean | |
| 700 | 1 | _aClaustres, Mireille | |
| 700 | 1 | _aTranchant, Christine | |
| 700 | 1 | _aAnheim, Mathieu | |
| 700 | 1 | _aKoenig, Michel | |
| 773 | 0 |
_tJournal of neurology _gvol. 263 _gno. 8 _gp. 1552-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s00415-016-8167-3 _zAvailable from publisher's website |
| 999 |
_c26064072 _d26064072 |
||