3-hydroxyacyl-CoA dehydrogenase (HAD) deficiency replaces short-chain hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency as well as medium- and short-chain hydroxyacyl-CoA dehydrogenase (M/SCHAD) deficiency as the consensus name of this fatty acid oxidation disorder.

MLA

He, Xue-Ying, and Song-Yu Yang. “3-Hydroxyacyl-CoA Dehydrogenase (HAD) Deficiency Replaces Short-Chain Hydroxyacyl-CoA Dehydrogenase (SCHAD) Deficiency as Well as Medium- and Short-Chain Hydroxyacyl-CoA Dehydrogenase (M/SCHAD) Deficiency as the Consensus Name of This Fatty Acid Oxidation Disorder.” Molecular Genetics and Metabolism, vol. 91, no. 2, June 2007, pp. 205–06. EBSCOhost, https://doi.org/10.1016/j.ymgme.2007.02.015.

APA

He, X.-Y., & Yang, S.-Y. (2007). 3-hydroxyacyl-CoA dehydrogenase (HAD) deficiency replaces short-chain hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency as well as medium- and short-chain hydroxyacyl-CoA dehydrogenase (M/SCHAD) deficiency as the consensus name of this fatty acid oxidation disorder. Molecular Genetics and Metabolism, 91(2), 205–206. https://doi.org/10.1016/j.ymgme.2007.02.015

Chicago

He, Xue-Ying, and Song-Yu Yang. 2007. “3-Hydroxyacyl-CoA Dehydrogenase (HAD) Deficiency Replaces Short-Chain Hydroxyacyl-CoA Dehydrogenase (SCHAD) Deficiency as Well as Medium- and Short-Chain Hydroxyacyl-CoA Dehydrogenase (M/SCHAD) Deficiency as the Consensus Name of This Fatty Acid Oxidation Disorder.” Molecular Genetics and Metabolism 91 (2): 205–6. doi:10.1016/j.ymgme.2007.02.015.