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SLC12A6 gene mutation
Clinical significance:
- see SLC12A6 & ACCPN*
* agenesis of the corpus callosum with peripheral neuropathy
Related
solute carrier family 12 member 6; electroneutral K+-chloride cotransporter 3; K-Cl cotransporter 3 (SLC12A6, KCC3)
General
gene mutation testing; gene mutation analysis
References
Loinc