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Pediatr Res 18:13251328 Roe CR, Millington DS, Maltby DA, Bohan TP, Kahler SG, Chalmers RA (1985) Diagnostic and therapeutic implications of medium-chain acylcarnitines in the medium-chain acyl-coA dehydrogenase deficiency
[Hepatology] 31
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For larger doses or when working with low concentrations that require drawing more than 50 units, use a 1 mL syringe (100 units max)
The protonation state of the latter is not strictly necessary to impart to the metal-thiolate core its electrical charge (calculated as 3 [155]) and can be changing
If an individual inherits one normal gene and one mutated gene, they will be a carrier but usually will not show any symptoms
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