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SLITRK6 - SLIT and NTRK like family member 6
- Disease-causing germline mutation(s) (loss of function) in Autosomal recessive non-syndromic sensorineural deafness type DFNB
- Disease-causing germline mutation(s) (loss of function) in High myopia-sensorineural deafness syndrome
Gene included in a panel of genes performed as part of a diagnostic test
Health care resources for this gene
Specialised Social Services
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