The first three years of screening for medium chain acyl-CoA dehydrogenase deficiency (MCADD) by newborn screening ontario
<p>Abstract</p> <p>Background</p> <p>Medium chain acyl-CoA dehydrogenase deficiency (MCADD) is a disorder of mitochondrial fatty acid oxidation and is one of the most common inborn errors of metabolism. Identification of MCADD via newborn screening permits the introduct...
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| Main Authors: | , , , , , , |
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| Format: | Book |
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BMC,
2010-11-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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