| 000 | 01625 a2200433 4500 | ||
|---|---|---|---|
| 005 | 20250516173938.0 | ||
| 264 | 0 | _c20140929 | |
| 008 | 201409s 0 0 eng d | ||
| 022 | _a1558-1497 | ||
| 024 | 7 |
_a10.1016/j.neurobiolaging.2013.09.016 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aLe Ber, Isabelle | |
| 245 | 0 | 0 |
_ahnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes. _h[electronic resource] |
| 260 |
_bNeurobiology of aging _cApr 2014 |
||
| 300 |
_a934.e5-6 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAmyotrophic Lateral Sclerosis _xgenetics |
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 |
_aFrontotemporal Lobar Degeneration _xgenetics |
| 650 | 0 | 4 | _aHeterogeneous Nuclear Ribonucleoprotein A1 |
| 650 | 0 | 4 |
_aHeterogeneous-Nuclear Ribonucleoprotein Group A-B _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aMyositis, Inclusion Body _xgenetics |
| 650 | 0 | 4 |
_aOsteitis Deformans _xgenetics |
| 700 | 1 | _aVan Bortel, Inge | |
| 700 | 1 | _aNicolas, Gael | |
| 700 | 1 | _aBouya-Ahmed, Kawtar | |
| 700 | 1 | _aCamuzat, Agnès | |
| 700 | 1 | _aWallon, David | |
| 700 | 1 | _aDe Septenville, Anne | |
| 700 | 1 | _aLatouche, Morwena | |
| 700 | 1 | _aLattante, Serena | |
| 700 | 1 | _aKabashi, Edor | |
| 700 | 1 | _aJornea, Ludmila | |
| 700 | 1 | _aHannequin, Didier | |
| 700 | 1 | _aBrice, Alexis | |
| 773 | 0 |
_tNeurobiology of aging _gvol. 35 _gno. 4 _gp. 934.e5-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.neurobiolaging.2013.09.016 _zAvailable from publisher's website |
| 999 |
_c23165318 _d23165318 |
||