000 01201 a2200337 4500
005 20250517033324.0
264 0 _c20160726
008 201607s 0 0 eng d
022 _a0722-5091
024 7 _a10.5414/NP300863
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aChang, Ki-Eun
245 0 0 _aType II (adult onset) Alexander disease in a paraplegic male with a rare D128N mutation in the GFAP gene.
_h[electronic resource]
260 _bClinical neuropathology
_c
300 _a298-302 p.
_bdigital
500 _aPublication Type: Case Reports; Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650 0 4 _aAlexander Disease
_xcomplications
650 0 4 _aGlial Fibrillary Acidic Protein
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aParaplegia
_xcomplications
700 1 _aPratt, Drew
700 1 _aMishra, Bibhuti B
700 1 _aEdwards, Nancy
700 1 _aHallett, Mark
700 1 _aRay-Chaudhury, Abhik
773 0 _tClinical neuropathology
_gvol. 34
_gno. 5
_gp. 298-302
856 4 0 _uhttps://doi.org/10.5414/NP300863
_zAvailable from publisher's website
999 _c24923285
_d24923285