Associated Papers
A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family.
Salime S et al.
Gene, 2018
BRAF alteration status and the histone H3F3A gene K27M mutation segregate spinal cord astrocytoma histology.
Shankar GM et al.
Acta Neuropathologica, 2016
26487540 (PubMed )
Supplement: 401_2015_1492_MOESM2_ESM.xlsx › Shankar_STable2
SLITRK6 mutations cause myopia and deafness in humans and mice.
Tekin M et al.
The Journal of Clinical Investigation, 2013
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