Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.

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Title:	Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
Author(s):	Ahmed, Z.M.; Masmoudi, S.; Kalay, E.; Belyantseva, I.A.; Mosrati, M.A.; Collin, R.W.J. ; Hmani-Aifa, M.; Venselaar, H. ; Kawar, M.N.; Tlili, A.; Zwaag, B. van der; Khan, S.; Ayadi, L.; Riazuddin, S.A.; Morell, R.J.; Griffith, A.J.; Charfedine, I.; Caylan, R.; Oostrik, J. ; Karaguzel, A.; Ghorbel, A.; Friedman, T.B.; Ayadi, H.; Kremer, H.
Publication year:	2008
Source:	Nature Genetics, vol. 40, iss. 11, (2008), pp. 1335-1340
ISSN:	1061-4036
DOI:	https://doi.org/10.1038/ng.245
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/70832
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Subject:	DCN 2: Functional Neurogenomics IGMD 3: Genomic disorders and inherited multi-system disorders NCMLS 3: Growth and differentiation NCMLS 6: Genetics and epigenetic pathways of disease UMCN 3.2: Cognitive neurosciences UMCN 3.3: Neurosensory disorders UMCN 5.1: Genetic defects of metabolism UMCN 5.1: Genetic defects of metabolism
Organization:	Human Genetics Otorhinolaryngology CMBI
Former Organization:	Bioinformatics (umcn)
Journal title:	Nature Genetics
Volume:	vol. 40
Issue:	iss. 11
Page start:	p. 1335
Page end:	p. 1340

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