000 01604 a2200409 4500
005 20250518084039.0
264 0 _c20210125
008 202101s 0 0 eng d
022 _a1873-474X
024 7 _a10.1002/jdn.10013
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSu, Tangfeng
245 0 0 _aEarly onset epileptic encephalopathy caused by novel compound heterozygous mutation of WWOX gene.
_h[electronic resource]
260 _bInternational journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
_cApr 2020
300 _a157-161 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAnticonvulsants
_xtherapeutic use
650 0 4 _aBrain Diseases
_xdrug therapy
650 0 4 _aElectroencephalography
650 0 4 _aEpilepsy
_xcomplications
650 0 4 _aFemale
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aMutation
_xgenetics
650 0 4 _aPrognosis
650 0 4 _aSpasms, Infantile
_xdrug therapy
650 0 4 _aTumor Suppressor Proteins
_xgenetics
650 0 4 _aWW Domain-Containing Oxidoreductase
_xgenetics
700 1 _aYan, Yu
700 1 _aXu, Shuang
700 1 _aZhang, Ke
700 1 _aXu, Sanqing
773 0 _tInternational journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
_gvol. 80
_gno. 2
_gp. 157-161
856 4 0 _uhttps://doi.org/10.1002/jdn.10013
_zAvailable from publisher's website
999 _c30614434
_d30614434