000 01338 a2200385 4500
005 20250518015902.0
264 0 _c20200505
008 202005s 0 0 eng d
022 _a1872-6968
024 7 _a10.1016/j.clineuro.2019.01.004
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aZhang, Chao
245 0 0 _aAtaxia with novel compound heterozygous PEX10 mutations and a literature review of PEX10-related peroxisome biogenesis disorders.
_h[electronic resource]
260 _bClinical neurology and neurosurgery
_c02 2019
300 _a92-96 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Review
650 0 4 _aCerebellar Ataxia
_xdiagnosis
650 0 4 _aChild
650 0 4 _aGenetic Testing
_xmethods
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
_xgenetics
650 0 4 _aPeroxins
_xgenetics
650 0 4 _aPeroxisomal Disorders
_xdiagnosis
650 0 4 _aReceptors, Cytoplasmic and Nuclear
_xgenetics
700 1 _aZhan, Fei-Xia
700 1 _aTian, Wo-Tu
700 1 _aXu, Yang-Qi
700 1 _aZhu, Ze-Yu
700 1 _aWang, Yan
700 1 _aSong, Xing-Wang
700 1 _aCao, Li
773 0 _tClinical neurology and neurosurgery
_gvol. 177
_gp. 92-96
856 4 0 _uhttps://doi.org/10.1016/j.clineuro.2019.01.004
_zAvailable from publisher's website
999 _c29251158
_d29251158