000 01635 a2200505 4500
005 20250517141630.0
264 0 _c20180115
008 201801s 0 0 eng d
022 _a1473-558X
024 7 _a10.1097/WNR.0000000000000754
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRaghuram, Vijeta
245 0 0 _aAssessment of mutations in KCNN2 and ZNF135 to patient neurological symptoms.
_h[electronic resource]
260 _bNeuroreport
_cMay 2017
300 _a375-379 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aAnimals
650 0 4 _aCRISPR-Cas Systems
650 0 4 _aCohort Studies
650 0 4 _aFemale
650 0 4 _aGene Editing
650 0 4 _aGene Knock-In Techniques
650 0 4 _aHEK293 Cells
650 0 4 _aHippocampus
_xmetabolism
650 0 4 _aHumans
650 0 4 _aMice, Inbred C57BL
650 0 4 _aMice, Transgenic
650 0 4 _aMotor Activity
_xphysiology
650 0 4 _aMutagenesis, Site-Directed
650 0 4 _aMutation
650 0 4 _aNervous System Diseases
_xgenetics
650 0 4 _aRNA, Messenger
_xmetabolism
650 0 4 _aRepressor Proteins
_xgenetics
650 0 4 _aSmall-Conductance Calcium-Activated Potassium Channels
_xgenetics
650 0 4 _aTissue Culture Techniques
700 1 _aWeber, Sydney
700 1 _aRaber, Jacob
700 1 _aChen, Dong-Hui
700 1 _aBird, Thomas D
700 1 _aMaylie, James
700 1 _aAdelman, John P
773 0 _tNeuroreport
_gvol. 28
_gno. 7
_gp. 375-379
856 4 0 _uhttps://doi.org/10.1097/WNR.0000000000000754
_zAvailable from publisher's website
999 _c26917077
_d26917077