| 000 | 01837 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250517040629.0 | ||
| 264 | 0 | _c20160810 | |
| 008 | 201608s 0 0 eng d | ||
| 022 | _a1559-1166 | ||
| 024 | 7 |
_a10.1007/s12031-015-0606-6 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aScimone, Concetta | |
| 245 | 0 | 0 |
_aDetection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations. _h[electronic resource] |
| 260 |
_bJournal of molecular neuroscience : MN _cNov 2015 |
||
| 300 |
_a400-3 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAmino Acid Motifs |
| 650 | 0 | 4 | _aAmino Acid Substitution |
| 650 | 0 | 4 |
_aApoptosis Regulatory Proteins _xgenetics |
| 650 | 0 | 4 |
_aCarrier Proteins _xgenetics |
| 650 | 0 | 4 | _aConserved Sequence |
| 650 | 0 | 4 |
_aGait Disorders, Neurologic _xetiology |
| 650 | 0 | 4 |
_aHemangioma, Cavernous, Central Nervous System _xcomplications |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aKRIT1 Protein |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMembrane Proteins _xgenetics |
| 650 | 0 | 4 |
_aMicrotubule-Associated Proteins _xgenetics |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 |
_aNeovascularization, Physiologic _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 |
_aProto-Oncogene Proteins _xgenetics |
| 650 | 0 | 4 |
_aVision Disorders _xetiology |
| 700 | 1 | _aBramanti, Placido | |
| 700 | 1 | _aRuggeri, Alessia | |
| 700 | 1 | _aKatsarou, Zoe | |
| 700 | 1 | _aDonato, Luigi | |
| 700 | 1 | _aSidoti, Antonina | |
| 700 | 1 | _aD'Angelo, Rosalia | |
| 773 | 0 |
_tJournal of molecular neuroscience : MN _gvol. 57 _gno. 3 _gp. 400-3 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s12031-015-0606-6 _zAvailable from publisher's website |
| 999 |
_c25021171 _d25021171 |
||