| 000 | 01534 a2200469 4500 | ||
|---|---|---|---|
| 005 | 20250516175730.0 | ||
| 264 | 0 | _c20140121 | |
| 008 | 201401s 0 0 eng d | ||
| 022 | _a1526-632X | ||
| 024 | 7 |
_a10.1212/01.wnl.0000436615.58705.c9 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMademan, Inès | |
| 245 | 0 | 0 |
_aDe novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy. _h[electronic resource] |
| 260 |
_bNeurology _cNov 2013 |
||
| 300 |
_a1953-8 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aCharcot-Marie-Tooth Disease _xcomplications |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFormins |
| 650 | 0 | 4 |
_aGlomerulosclerosis, Focal Segmental _xcomplications |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMicrofilament Proteins _xgenetics |
| 650 | 0 | 4 | _aModels, Molecular |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aDeconinck, Tine | |
| 700 | 1 | _aDinopoulos, Argirios | |
| 700 | 1 | _aVoit, Thomas | |
| 700 | 1 | _aSchara, Ulrike | |
| 700 | 1 | _aDevriendt, Koenraad | |
| 700 | 1 | _aMeijers, Björn | |
| 700 | 1 | _aLerut, Evelyne | |
| 700 | 1 | _aDe Jonghe, Peter | |
| 700 | 1 | _aBaets, Jonathan | |
| 773 | 0 |
_tNeurology _gvol. 81 _gno. 22 _gp. 1953-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1212/01.wnl.0000436615.58705.c9 _zAvailable from publisher's website |
| 999 |
_c23215618 _d23215618 |
||