| 000 | 01773 a2200553 4500 | ||
|---|---|---|---|
| 005 | 20250516204408.0 | ||
| 264 | 0 | _c20140401 | |
| 008 | 201404s 0 0 eng d | ||
| 022 | _a2324-9269 | ||
| 024 | 7 |
_a10.1002/mgg3.60 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSpiegler, Stefanie | |
| 245 | 0 | 0 |
_aHigh mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one-third of probands are minors. _h[electronic resource] |
| 260 |
_bMolecular genetics & genomic medicine _cMar 2014 |
||
| 300 |
_a176-85 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 700 | 1 | _aNajm, Juliane | |
| 700 | 1 | _aLiu, Jian | |
| 700 | 1 | _aGkalympoudis, Stephanie | |
| 700 | 1 | _aSchröder, Winnie | |
| 700 | 1 | _aBorck, Guntram | |
| 700 | 1 | _aBrockmann, Knut | |
| 700 | 1 | _aElbracht, Miriam | |
| 700 | 1 | _aFauth, Christine | |
| 700 | 1 | _aFerbert, Andreas | |
| 700 | 1 | _aFreudenberg, Leonie | |
| 700 | 1 | _aGrasshoff, Ute | |
| 700 | 1 | _aHellenbroich, Yorck | |
| 700 | 1 | _aHenn, Wolfram | |
| 700 | 1 | _aHoffjan, Sabine | |
| 700 | 1 | _aHüning, Irina | |
| 700 | 1 | _aKorenke, G Christoph | |
| 700 | 1 | _aKroisel, Peter M | |
| 700 | 1 | _aKunstmann, Erdmute | |
| 700 | 1 | _aMair, Martina | |
| 700 | 1 | _aMunk-Schulenburg, Susanne | |
| 700 | 1 | _aNikoubashman, Omid | |
| 700 | 1 | _aPauli, Silke | |
| 700 | 1 | _aRudnik-Schöneborn, Sabine | |
| 700 | 1 | _aSudholt, Irene | |
| 700 | 1 | _aSure, Ulrich | |
| 700 | 1 | _aTinschert, Sigrid | |
| 700 | 1 | _aWiednig, Michaela | |
| 700 | 1 | _aZoll, Barbara | |
| 700 | 1 | _aGinsberg, Mark H | |
| 700 | 1 | _aFelbor, Ute | |
| 773 | 0 |
_tMolecular genetics & genomic medicine _gvol. 2 _gno. 2 _gp. 176-85 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/mgg3.60 _zAvailable from publisher's website |
| 999 |
_c23695907 _d23695907 |
||