000 01236 a2200289 4500
005 20250515011849.0
264 0 _c20060630
008 200606s 0 0 eng d
022 _a1096-7192
024 7 _a10.1016/j.ymgme.2005.10.019
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSchiffmann, Raphael
245 0 0 _aChildhood ataxia with CNS hypomyelination/vanishing white matter disease--a common leukodystrophy caused by abnormal control of protein synthesis.
_h[electronic resource]
260 _bMolecular genetics and metabolism
_cMay 2006
300 _a7-15 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Review
650 0 4 _aBrain
_xpathology
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aEukaryotic Initiation Factor-2B
_xdeficiency
650 0 4 _aHumans
650 0 4 _aMagnetic Resonance Imaging
650 0 4 _aSpinocerebellar Degenerations
_xdiagnosis
700 1 _aElroy-Stein, Orna
773 0 _tMolecular genetics and metabolism
_gvol. 88
_gno. 1
_gp. 7-15
856 4 0 _uhttps://doi.org/10.1016/j.ymgme.2005.10.019
_zAvailable from publisher's website
999 _c15997189
_d15997189