RS104894715 PRX
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive Dejerine-Sottas syndrome
Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4F
Peripheral neuropathy
Inborn genetic diseases
Autosomal recessive Dejerine-Sottas syndrome
Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4F
Peripheral neuropathy
Inborn genetic diseases
Other Variants in PRX