SLC12A6 gene mutation

Clinical significance

• see SLC12A6 & ACCPN*

* agenesis of the corpus callosum with peripheral neuropathy

More general terms

• gene mutation testing; gene mutation analysis

Additional terms

• solute carrier family 12 member 6; electroneutral K+-chloride cotransporter 3; K-Cl cotransporter 3 (SLC12A6, KCC3)