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GENATLAS PHENOTYPE

last update : 15-01-2010

Symbol	DICMT3
Location	16q22.1
Name	dominant intermediate Charcot-Marie-Tooth neuropathy 3
Corresponding gene	AARS
Main clinical features	progressive weakness and atrophy, initially of the peroneal muscles and later of the distal muscles of the arms at EMG, motor and sensory denervation
Genetic determination	autosomal dominant
Function/system disorder	neuromuscular
Type	disease

Remark(s)