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#614895 - CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F
Cytogenetic locations: 22847150
Gene summaries Genetic tests Medical literature
*605725 - PERIAXIN; PRX
#145900 - HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS
Cytogenetic locations: 1p36, 1p36, 1p36
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