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