id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_qlnxkowworhf7g47acyzzdlssq	Mustafa Tekin	SLITRK6 mutations cause myopia and deafness in humans and mice	2013.0	10	.pdf	application/pdf	7627	720	57	SLITRK6 mutations cause myopia and deafness in humans and of WT and Slitrk6-deficient mouse eyes revealed axial length increase in the mutant (the endophenotype of myopia). Taken together, our results showed that SLITRK6 plays a crucial role in the development of normal hearing as High-resolution MRI of WT and Slitrk6-deficient mouse eyes revealed axial length increase results showed that SLITRK6 plays a crucial role in the development of normal hearing as well as vision in SLITRK6 mutations cause high myopia and sensorineural deafness in apparent in newborn mice, as determined in serial sections of freshly frozen eyes (Figure 3), which indicates that SLITRK6 regulates Increased axial length of the eyes of Slitrk6 KO mice. high myopia and sensorineural deafness as the only clinical findings and confirmed a similar phenotype in Slitrk6 mutant mice. myopia — such as cataract, glaucoma, and chorioretinal abnormalities — in either humans or mice; therefore, the Slitrk6 KO mouse 	./cache/work_qlnxkowworhf7g47acyzzdlssq.pdf	./txt/work_qlnxkowworhf7g47acyzzdlssq.txt