Article ID Journal Published Year Pages File Type
9888289 Clinica Chimica Acta 2005 5 Pages PDF
Abstract
We established the molecular basis of butyrylcholinesterase deficiency in two Chinese patients. The developed mutation detection assay provides a reliable method for identifying mutant BCHE carriers.
Keywords
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Biochemistry
Preview
Novel mutations in the BCHE gene in patients with no butyrylcholinesterase activity
Authors
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