Associated Papers
Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss.
Sheppard S et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2018
29907799 (PubMed )
Supplement: 41436_2018_4_MOESM3_ESM.xlsx › variant-_capture___coverage
A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family.
Salime S et al.
Gene, 2018
A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humans.
Morlet T et al.
The Laryngoscope, 2014
SLITRK6 mutations cause myopia and deafness in humans and mice.
Tekin M et al.
The Journal of Clinical Investigation, 2013
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