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KIF1B - kinesin family member 1B
- Disease-causing germline mutation(s) (loss of function) in Autosomal dominant Charcot-Marie-Tooth disease type 2A1
- Disease-causing germline mutation(s) (loss of function) in Hereditary pheochromocytoma-paraganglioma
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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