Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer (UCN) gene.

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Title:	Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer (UCN) gene.
Author(s):	Verhoeven, K.; Ensink, R.J.H. ; Tiranti, V.; Huygen, P.L.M. ; Johnson, D.F.; Schatteman, I.; Laer, L. van; Verstreken, M.; Heyning, P. van de; Fischel-Ghodsian, N.; Zeviani, M.; Cremers, C.W.R.J. ; Willems, P.H.G.M. ; Camp, G. van
Publication year:	1999
Source:	European Journal of Human Genetics, vol. 7, (1999), pp. 45-51
ISSN:	1018-4813
DOI:	https://doi.org/10.1038/sj.ejhg.5200247
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/189339
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Subject:	Genetics of hearing Erfelijk gehoorverlies
Organization:	Otorhinolaryngology Cell Biology (UMC)
Journal title:	European Journal of Human Genetics
Volume:	vol. 7
Page start:	p. 45
Page end:	p. 51