000 | 01694 a2200493 4500 | ||
---|---|---|---|
005 | 20250515160148.0 | ||
264 | 0 | _c20090728 | |
008 | 200907s 0 0 eng d | ||
022 | _a1531-8257 | ||
024 | 7 |
_a10.1002/mds.22467 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aDemos, Michelle K | |
245 | 0 | 0 |
_aA novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction. _h[electronic resource] |
260 |
_bMovement disorders : official journal of the Movement Disorder Society _cApr 2009 |
||
300 |
_a778-82 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAnimals |
650 | 0 | 4 | _aCHO Cells |
650 | 0 | 4 |
_aCerebellar Diseases _xgenetics |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 | _aCricetinae |
650 | 0 | 4 | _aCricetulus |
650 | 0 | 4 |
_aDNA Mutational Analysis _xmethods |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGenetic Predisposition to Disease |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aKv1.1 Potassium Channel _xgenetics |
650 | 0 | 4 |
_aLeucine _xgenetics |
650 | 0 | 4 |
_aMagnetic Resonance Imaging _xmethods |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aMembrane Potentials _xgenetics |
650 | 0 | 4 |
_aMutation _xgenetics |
650 | 0 | 4 |
_aTransfection _xmethods |
650 | 0 | 4 |
_aValine _xgenetics |
700 | 1 | _aMacri, Vincenzo | |
700 | 1 | _aFarrell, Kevin | |
700 | 1 | _aNelson, Tanya N | |
700 | 1 | _aChapman, Kristine | |
700 | 1 | _aAccili, Eric | |
700 | 1 | _aArmstrong, Linlea | |
773 | 0 |
_tMovement disorders : official journal of the Movement Disorder Society _gvol. 24 _gno. 5 _gp. 778-82 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1002/mds.22467 _zAvailable from publisher's website |
999 |
_c18649077 _d18649077 |