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Andermann syndrome (Charlevoix' disease)
Genetics:
- mutation in gene for solute carrier family 12 member 6
Related
solute carrier family 12 member 6; electroneutral K+-chloride cotransporter 3; K-Cl cotransporter 3 (SLC12A6, KCC3)
spastic ataxia of Charlevoix-Saguenay
General
inborn error of metabolism
Database Correlations
OMIM 218000
References
OMIM :accession 218000