000 01476 a2200469 4500
005 20250515151938.0
264 0 _c20090408
008 200904s 0 0 eng d
022 _a1708-8283
024 7 _a10.1177/0883073808320754
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGregory, Mary L
245 0 0 _aA novel GLRA1 mutation associated with an atypical hyperekplexia phenotype.
_h[electronic resource]
260 _bJournal of child neurology
_cDec 2008
300 _a1433-8 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdult
650 0 4 _aBlack or African American
650 0 4 _aArginine
_xgenetics
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aChromosomes, Human, Pair 5
650 0 4 _aDNA Mutational Analysis
_xmethods
650 0 4 _aFamily Health
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMuscle Hypertonia
_xgenetics
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aProline
_xgenetics
650 0 4 _aReceptors, Glycine
_xgenetics
650 0 4 _aReflex, Abnormal
_xgenetics
700 1 _aGuzauskas, Greg F
700 1 _aEdgar, Terence S
700 1 _aClarkson, Kate B
700 1 _aSrivastava, Anand K
700 1 _aHolden, Kenton R
773 0 _tJournal of child neurology
_gvol. 23
_gno. 12
_gp. 1433-8
856 4 0 _uhttps://doi.org/10.1177/0883073808320754
_zAvailable from publisher's website
999 _c18526612
_d18526612