| 000 | 01242 a2200373 4500 | ||
|---|---|---|---|
| 005 | 20250517012907.0 | ||
| 264 | 0 | _c20160627 | |
| 008 | 201606s 0 0 eng d | ||
| 022 | _a1399-0004 | ||
| 024 | 7 |
_a10.1111/cge.12554 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKanbayashi, Takamichi | |
| 245 | 0 | 0 |
_aAdult-onset vanishing white matter disease with novel missense mutations in a subunit of translational regulator, EIF2B4. _h[electronic resource] |
| 260 |
_bClinical genetics _cOct 2015 |
||
| 300 |
_a401-3 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Letter | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aEukaryotic Initiation Factor-2B _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Association Studies |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aLeukoencephalopathies _xgenetics |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aMutation, Missense |
| 700 | 1 | _aSaito, Fumiaki | |
| 700 | 1 | _aMatsukawa, Takashi | |
| 700 | 1 | _aOba, Hiroshi | |
| 700 | 1 | _aHokkoku, Keiichi | |
| 700 | 1 | _aHatanaka, Yuki | |
| 700 | 1 | _aTsuji, Shoji | |
| 700 | 1 | _aSonoo, Masahiro | |
| 773 | 0 |
_tClinical genetics _gvol. 88 _gno. 4 _gp. 401-3 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/cge.12554 _zAvailable from publisher's website |
| 999 |
_c24544894 _d24544894 |
||