| 000 | 01129 a2200325 4500 | ||
|---|---|---|---|
| 005 | 20250518091821.0 | ||
| 264 | 0 | _c20210531 | |
| 008 | 202105s 0 0 eng d | ||
| 022 | _a2240-2993 | ||
| 024 | 7 |
_a10.1007/s13760-020-01329-y _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aNoushad, Muhammed | |
| 245 | 0 | 0 |
_aA British family with familial cerebral cavernous malformation due to a rare mutation of the CCM2 gene. _h[electronic resource] |
| 260 |
_bActa neurologica Belgica _cOct 2020 |
||
| 300 |
_a1227-1229 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Letter | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aCarrier Proteins _xgenetics |
| 650 | 0 | 4 | _aCodon, Nonsense |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aHemangioma, Cavernous, Central Nervous System _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPedigree |
| 700 | 1 | _aBhattacharjee, Shakya | |
| 700 | 1 | _aWeatherby, Stuart J | |
| 700 | 1 | _aWhitefield, Peter | |
| 773 | 0 |
_tActa neurologica Belgica _gvol. 120 _gno. 5 _gp. 1227-1229 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s13760-020-01329-y _zAvailable from publisher's website |
| 999 |
_c30740819 _d30740819 |
||