000 01266 a2200397 4500
005 20250517114704.0
264 0 _c20180209
008 201802s 0 0 eng d
022 _a1364-6753
024 7 _a10.1007/s10048-016-0491-3
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCohen, Rony
245 0 0 _aPolymicrogyria and myoclonic epilepsy in autosomal recessive cutis laxa type 2A.
_h[electronic resource]
260 _bNeurogenetics
_c10 2016
300 _a251-257 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aBrain
_xdiagnostic imaging
650 0 4 _aChild
650 0 4 _aCutis Laxa
_xcomplications
650 0 4 _aEpilepsies, Myoclonic
_xcomplications
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPolymicrogyria
_xcomplications
650 0 4 _aSiblings
700 1 _aHalevy, Ayelet
700 1 _aAharoni, Sharon
700 1 _aKraus, Dror
700 1 _aKonen, Osnat
700 1 _aBasel-Vanagaite, Lina
700 1 _aGoldberg-Stern, Hadassa
700 1 _aStraussberg, Rachel
773 0 _tNeurogenetics
_gvol. 17
_gno. 4
_gp. 251-257
856 4 0 _uhttps://doi.org/10.1007/s10048-016-0491-3
_zAvailable from publisher's website
999 _c26421855
_d26421855