000			01722 a2200553 4500
005			20250515203054.0
264		0	_c20100310
008			201003s 0 0 eng d
022			_a1090-0535
040			_aNLM _beng _cNLM
100	1		_aHogewind, Barend F T
245	0	0	_aAutosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1. _h[electronic resource]
260			_bMolecular vision _cJan 2010
300			_a26-35 p. _bdigital
500			_aPublication Type: Journal Article
650	0	4	_aAdult
650	0	4	_aAged, 80 and over
650	0	4	_aAmino Acid Sequence
650	0	4	_aBase Sequence
650	0	4	_aConserved Sequence
650	0	4	_aDNA Mutational Analysis
650	0	4	_aDiabetes Mellitus _xgenetics
650	0	4	_aEvolution, Molecular
650	0	4	_aFamily
650	0	4	_aFemale
650	0	4	_aGenes, Dominant _xgenetics
650	0	4	_aGenetic Association Studies
650	0	4	_aGenetic Predisposition to Disease
650	0	4	_aHearing Loss, Sensorineural _xcomplications
650	0	4	_aHearing Tests
650	0	4	_aHumans
650	0	4	_aMale
650	0	4	_aMembrane Proteins _xchemistry
650	0	4	_aMiddle Aged
650	0	4	_aMolecular Sequence Data
650	0	4	_aMutation _xgenetics
650	0	4	_aOcular Physiological Phenomena
650	0	4	_aOptic Nerve Diseases _xcomplications
650	0	4	_aPedigree
650	0	4	_aPhenotype
650	0	4	_aYoung Adult
700	1		_aPennings, Ronald J E
700	1		_aHol, Frans A
700	1		_aKunst, Henricus P M
700	1		_aHoefsloot, Elisabeth H
700	1		_aCruysberg, Johannes R M
700	1		_aCremers, Cor W R J
773	0		_tMolecular vision _gvol. 16 _gp. 26-35
999			_c19447315 _d19447315