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Description
Distinctive structure of the human GSTM3 gene-inverted orientation relative to the mu class glutathione transferase gene cluster
M.IngramS
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Background: GNAO1 associated encephalopathy is an autosomal dominant disorder caused by mutation/s in GNAO1 gene that encodes subunit of guanine nucleotidebinding proteins (Go) which are highly expressed in brain and modulate the neuronal excitability
3 and 4, respectively
