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#620068 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2II; CMT2II
Cytogenetic locations: 616605
Gene summaries Genetic tests Medical literature
*604878 - SOLUTE CARRIER FAMILY 12 (POTASSIUM/CHLORIDE TRANSPORTER), MEMBER 6; SLC12A6
POTASSIUM-CHLORIDE COTRANSPORTER 3, ISOFORM A, INCLUDED; KCC3A, INCLUDED
#218000 - AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN
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