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Description
Ethics approval College of Science Ethics Committee, University of Babylon, Iraq
L-2-HGA is an autosomal recessive encephalopathy with an onset in childhood that causes developmental delays, epilepsy and cerebellar ataxia, the traditional clinical signs of this condition
It is concluded that the GPs may also order the GGT test as a direct tool to prognosis the early HF condition in patients suffering from cardiac muscle disorders
npr , ahpC , ahpF , encoding peroxidases
