Tekin, M; Chioza, BA; Matsumoto, Y; Diaz-Horta, O; Cross, HE; Duman, D; Kokotas, H; Moore-Barton, HL; Sakoori, K; Ota, M; et al. Tekin, M; Chioza, BA; Matsumoto, Y; Diaz-Horta, O; Cross, HE; Duman, D; Kokotas, H; Moore-Barton, HL; Sakoori, K; Ota, M; Odaka, YS; Foster, J; Cengiz, FB; Tokgoz-Yilmaz, S; Tekeli, O; Grigoriadou, M; Petersen, MB; Sreekantan-Nair, A; Gurtz, K; Xia, XJ; Pandya, A; Patton, MA; Young, JI; Aruga, J; Crosby, AH (2013) SLITRK6 mutations cause myopia and deafness in humans and mice. JOURNAL OF CLINICAL INVESTIGATION, 123 (5). 2094 - 2102 (9). ISSN 0021-9738 https://doi.org/10.1172/JCI65853
SGUL Authors: Chioza, Barry Andrew Patton, Michael Alexander Sreekantan Nair, Ajith

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Item Type:	Article
Additional Information:	PubMed ID: 23543054
Keywords:	Adolescent, Adult, Animals, Child, Codon, Nonsense, Female, Hearing, Hearing Loss, Sensorineural, Humans, Infant, Male, Membrane Proteins, Mice, Mice, Knockout, Middle Aged, Mutation, Myopia, Pedigree, Phenotype, Protein Structure, Tertiary, Young Adult, Science & Technology, Life Sciences & Biomedicine, Medicine, Research & Experimental, Research & Experimental Medicine, GENOME-WIDE ASSOCIATION, DNA-SEQUENCING DATA, REFRACTIVE ERROR, SUSCEPTIBILITY LOCUS, EXPRESSION, MOUSE, HERITABILITY, PREVALENCE, FRAMEWORK, GENETICS
SGUL Research Institute / Research Centre:	Academic Structure > Institute of Medical & Biomedical Education (IMBE) Academic Structure > Institute of Medical & Biomedical Education (IMBE) > Centre for Clinical Education (INMECE )
Journal or Publication Title:	JOURNAL OF CLINICAL INVESTIGATION
ISSN:	0021-9738
Dates:	Date Event 1 May 2013 Published
PubMed ID:	23543054
Web of Science ID:	23543054
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URI:	https://openaccess.sgul.ac.uk/id/eprint/101675
Publisher's version:	https://doi.org/10.1172/JCI65853

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