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#617882 - CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG
Cytogenetic locations: 14733962
Gene summaries Genetic tests Medical literature
#607734 - CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F
Cytogenetic locations: 20039262
#607684 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E
Cytogenetic locations: 17881652
*162280 - NEUROFILAMENT PROTEIN, LIGHT POLYPEPTIDE; NEFL
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