Research

Al-Walid A. Mohsen, PhD, Research Projects

Medium chain acyl-CoA dehydrogenase deficiency (MCADD) is an inborn error of fatty acid metabolism, rivaling phenylalanine hydroxylase deficiency (PKU) as the most common biochemical genetic disorder and one of several targeted by Al-Walid A. Mohsen, PhD.

Summaries of his current work are listed below.

Last Update
August 14, 2010
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Last Update
August 14, 2010
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