000			02101 a2200661 4500
005			20250516082443.0
264		0	_c20120713
008			201207s 0 0 eng d
022			_a1537-6605
024	7		_a10.1016/j.ajhg.2012.02.007 _2doi
040			_aNLM _beng _cNLM
100	1		_aHoyer, Juliane
245	0	0	_aHaploinsufficiency of ARID1B, a member of the SWI/SNF-a chromatin-remodeling complex, is a frequent cause of intellectual disability. _h[electronic resource]
260			_bAmerican journal of human genetics _cMar 2012
300			_a565-72 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAdolescent
650	0	4	_aAdult
650	0	4	_aChild
650	0	4	_aChild, Preschool
650	0	4	_aChromatin _xgenetics
650	0	4	_aChromatin Assembly and Disassembly _xgenetics
650	0	4	_aChromosomal Proteins, Non-Histone _xgenetics
650	0	4	_aCohort Studies
650	0	4	_aDNA Mutational Analysis _xmethods
650	0	4	_aDNA-Binding Proteins _xgenetics
650	0	4	_aExons
650	0	4	_aFemale
650	0	4	_aHaploinsufficiency
650	0	4	_aHumans
650	0	4	_aIntellectual Disability
650	0	4	_aMale
650	0	4	_aMiddle Aged
650	0	4	_aMutation
650	0	4	_aTranscription Factors _xgenetics
650	0	4	_aYoung Adult
700	1		_aEkici, Arif B
700	1		_aEndele, Sabine
700	1		_aPopp, Bernt
700	1		_aZweier, Christiane
700	1		_aWiesener, Antje
700	1		_aWohlleber, Eva
700	1		_aDufke, Andreas
700	1		_aRossier, Eva
700	1		_aPetsch, Corinna
700	1		_aZweier, Markus
700	1		_aGöhring, Ina
700	1		_aZink, Alexander M
700	1		_aRappold, Gudrun
700	1		_aSchröck, Evelin
700	1		_aWieczorek, Dagmar
700	1		_aRiess, Olaf
700	1		_aEngels, Hartmut
700	1		_aRauch, Anita
700	1		_aReis, André
773	0		_tAmerican journal of human genetics _gvol. 90 _gno. 3 _gp. 565-72
856	4	0	_uhttps://doi.org/10.1016/j.ajhg.2012.02.007 _zAvailable from publisher's website
999			_c21610406 _d21610406