Genetic and immunological analyses of patients with increased serum butyrylcholinesterase activity and its C5 variant form

Author:

Akizuki Setsuko,Ohnishi Akihiro,Kotani Kazuo,Sudo Kayoko

Abstract

AbstractRecent evidence has denied genetic abnormality as a mechanism of the C5 variant of butyrylcholinesterase (BChE) and proposed the binding of an unknown protein with the C4 component. The present study aimed to evaluate whether the coding sequences and nontranslated sequences of the

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry, medical,Clinical Biochemistry,General Medicine

Reference38 articles.

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5. der DNA mutation associated with the human butyrylcholinesterase variant and its linkage to the atypical variant mutation and other polymorphic sites;Bartels;Am J Hum Genet,1992

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