000 01539 a2200325 4500
005 20250515091106.0
264 0 _c20080723
008 200807s 0 0 eng d
022 _a1552-485X
024 7 _a10.1002/ajmg.b.30613
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBonnet-Dupeyron, Marie-Noelle
245 0 0 _aAbsence of OLIG2 mutations in patients presenting with a severe Pelizaeus-Merzbacher-like leukodystrophy associated with motor neuron dysfunction.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
_cJun 2008
300 _a538-9 p.
_bdigital
500 _aPublication Type: Letter; Research Support, Non-U.S. Gov't
650 0 4 _aBasic Helix-Loop-Helix Transcription Factors
_xgenetics
650 0 4 _aDemyelinating Diseases
650 0 4 _aHumans
650 0 4 _aMotor Neuron Disease
650 0 4 _aMutation
650 0 4 _aNerve Tissue Proteins
_xgenetics
650 0 4 _aOligodendrocyte Transcription Factor 2
650 0 4 _aPelizaeus-Merzbacher Disease
_xgenetics
700 1 _aCombes, Patricia
700 1 _aBoespflug-Tanguy, Odile
700 1 _aVaurs-Barrière, Catherine
773 0 _tAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
_gvol. 147B
_gno. 4
_gp. 538-9
856 4 0 _uhttps://doi.org/10.1002/ajmg.b.30613
_zAvailable from publisher's website
999 _c17439595
_d17439595