| 000 | 01651 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250515091625.0 | ||
| 264 | 0 | _c20080104 | |
| 008 | 200801s 0 0 eng d | ||
| 022 | _a0009-9163 | ||
| 024 | 7 |
_a10.1111/j.1399-0004.2007.00887.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aWatts, G D J | |
| 245 | 0 | 0 |
_aNovel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. _h[electronic resource] |
| 260 |
_bClinical genetics _cNov 2007 |
||
| 300 |
_a420-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAdenosine Triphosphatases _xgenetics |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aCell Cycle Proteins _xgenetics |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 |
_aDementia _xcomplications |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aModels, Molecular |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aMyositis, Inclusion Body _xcomplications |
| 650 | 0 | 4 |
_aOsteitis Deformans _xcomplications |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aValosin Containing Protein |
| 700 | 1 | _aThomasova, D | |
| 700 | 1 | _aRamdeen, S K | |
| 700 | 1 | _aFulchiero, E C | |
| 700 | 1 | _aMehta, S G | |
| 700 | 1 | _aDrachman, D A | |
| 700 | 1 | _aWeihl, C C | |
| 700 | 1 | _aJamrozik, Z | |
| 700 | 1 | _aKwiecinski, H | |
| 700 | 1 | _aKaminska, A | |
| 700 | 1 | _aKimonis, V E | |
| 773 | 0 |
_tClinical genetics _gvol. 72 _gno. 5 _gp. 420-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1399-0004.2007.00887.x _zAvailable from publisher's website |
| 999 |
_c17456072 _d17456072 |
||