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9, 1998, pp
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Suggest very low levels ( 2.5 mmol/l) are flagged to alert clinicians to the potential need to assess for secondary causes and inherited metabolic diseases (see Section 15)
Albinism is also framed in the negative through malady, narrated as having a genetic disease or congenital disorder instead of neutrally framing it as a genetic occurrence or congenital characteristic
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however, clinical trials have not shown significant improvement in attention post-TBI
