000 01226 a2200361 4500
005 20250515143802.0
264 0 _c20081219
008 200812s 0 0 eng d
022 _a0887-8994
024 7 _a10.1016/j.pediatrneurol.2008.07.030
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGuerin, Andrea A
245 0 0 _aStepwise developmental regression associated with novel CACNA1A mutation.
_h[electronic resource]
260 _bPediatric neurology
_cNov 2008
300 _a363-4 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAtaxia
_xgenetics
650 0 4 _aCalcium Channels
_xgenetics
650 0 4 _aChild
650 0 4 _aConsciousness Disorders
_xgenetics
650 0 4 _aEpilepsy
_xgenetics
650 0 4 _aFamily Health
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMigraine with Aura
_xgenetics
650 0 4 _aMutation, Missense
700 1 _aFeigenbaum, Annette
700 1 _aDonner, Elizabeth J
700 1 _aYoon, Grace
773 0 _tPediatric neurology
_gvol. 39
_gno. 5
_gp. 363-4
856 4 0 _uhttps://doi.org/10.1016/j.pediatrneurol.2008.07.030
_zAvailable from publisher's website
999 _c18403643
_d18403643