Biochemical and genetic analysis of butyrylcholinesterase (BChE) in a family, due to prolonged neuromuscular blockade after the use of succinylcholine

Author:

Garcia Daniel Fantozzi1,Oliveira Ticiano G.2,Molfetta Greice A.3,Garcia Luiz V.2,Ferreira Cristiane A.3,Marques Adriana A.3,Silva Jr. Wilson Araujo1

Affiliation:

1. Universidade de São Paulo, Brazil; Universidade de São Paulo, Brazil; Instituto Nacional de Ciência e Tecnologia em Terapia Celular e Centro de Terapia Celular, Brazil

2. Universidade de São Paulo, Brazil; Universidade de São Paulo, Brazil

3. Universidade de São Paulo, Brazil; Instituto Nacional de Ciência e Tecnologia em Terapia Celular e Centro de Terapia Celular, Brazil

Publisher

FapUNIFESP (SciELO)

Subject

Genetics,Molecular Biology

Reference17 articles.

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

2. The continuing search for a succinylcholine replacement;Caldwell JE;Anesthesiology,2004

3. Sensitivity to succinylcholine in relation to serum-cholinesterase;Evans FT;Lancet,1952

4. Association of variants of the -116 site of the butyrylcholinesterase BCHE gene to enzyme activity and body mass index;Furtado-Alle L;Chem Biol Interact,2008

5. A micro method for serum cholinesterase;Garry PJ;Clin Chem,1965

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