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GENATLAS PHENOTYPE

last update : 21/08/2006

Symbol	MTCYB
Location	mt
Name	mitochondrial encephalomyopathy
Corresponding gene	MT-CYB
related resource	MITOP database
Main clinical features	with exercice intolerance and lactic acidosis complex III deficiency
Genetic determination	mitochondrial
Function/system disorder	neurology
Type	disease

Gene product

Name	cytochrome B,complex III (nt15242 G->A)