000			02162 a2200733 4500
005			20250517020221.0
264		0	_c20160916
008			201609s 0 0 eng d
022			_a1476-5578
024	7		_a10.1038/mp.2015.5 _2doi
040			_aNLM _beng _cNLM
100	1		_avan Bon, B W M
245	0	0	_aDisruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. _h[electronic resource]
260			_bMolecular psychiatry _cJan 2016
300			_a126-32 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650	0	4	_aAdolescent
650	0	4	_aAdult
650	0	4	_aAutistic Disorder _xgenetics
650	0	4	_aChild
650	0	4	_aChild, Preschool
650	0	4	_aCohort Studies
650	0	4	_aFemale
650	0	4	_aFetal Growth Retardation _xgenetics
650	0	4	_aHumans
650	0	4	_aIntellectual Disability _xgenetics
650	0	4	_aMale
650	0	4	_aMicrocephaly _xgenetics
650	0	4	_aMiddle Aged
650	0	4	_aMutation
650	0	4	_aPhenotype
650	0	4	_aProtein Serine-Threonine Kinases _xgenetics
650	0	4	_aProtein-Tyrosine Kinases _xgenetics
650	0	4	_aSeizures, Febrile _xgenetics
650	0	4	_aSiblings
650	0	4	_aSpeech Disorders _xgenetics
650	0	4	_aStereotypic Movement Disorder _xgenetics
650	0	4	_aSyndrome
650	0	4	_aYoung Adult
650	0	4	_aDyrk Kinases
700	1		_aCoe, B P
700	1		_aBernier, R
700	1		_aGreen, C
700	1		_aGerdts, J
700	1		_aWitherspoon, K
700	1		_aKleefstra, T
700	1		_aWillemsen, M H
700	1		_aKumar, R
700	1		_aBosco, P
700	1		_aFichera, M
700	1		_aLi, D
700	1		_aAmaral, D
700	1		_aCristofoli, F
700	1		_aPeeters, H
700	1		_aHaan, E
700	1		_aRomano, C
700	1		_aMefford, H C
700	1		_aScheffer, I
700	1		_aGecz, J
700	1		_ade Vries, B B A
700	1		_aEichler, E E
773	0		_tMolecular psychiatry _gvol. 21 _gno. 1 _gp. 126-32
856	4	0	_uhttps://doi.org/10.1038/mp.2015.5 _zAvailable from publisher's website
999			_c24648014 _d24648014