Analysis of mutations in the plasma cholinesterase gene of patients with a history of prolonged neuromuscular block during anesthesia

Molecular Genetics and Metabolism

Volumn 74, Issue 4, 2001, Pages 484-488

  Barta, Csaba ^a   Sasvari Szekely, Maria ^a   Devai, Adrien ^b   Kovacs, Erika ^a   Staub, Maria ^a   Enyedi, Peter ^a  

^a SEMMELWEIS UNIVERSITY   (Hungary)

^b Bethesda Children's Hospital   (Hungary)

Author keywords

BCHE; PCR; Plasma cholinesterase; Prolonged neuromuscular block; Sequencing

Indexed keywords

CHOLINESTERASE; MIVACURIUM; SUXAMETHONIUM; VECURONIUM;

ARTICLE; CASE REPORT; CHOLINESTERASE BLOOD LEVEL; EXON; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENOTYPE; HUMAN; NEUROMUSCULAR BLOCKING; PEDIGREE; PRIORITY JOURNAL;

EID: 0035691732     PISSN: 10967192     EISSN: None     Source Type: Journal    
DOI: 10.1006/mgme.2001.3251     Document Type: Article

References (11)

1. Complete amino acid sequence of human serum cholinesterase
2. The structure of the active surface of serum cholinesterase
3. Identification of human plasma cholinesterase variants using molecular biological techniques
4. Genetic variants of human serum cholinesterase influence metabolism of the muscle relaxant succinylcholine
5. Cholinesterase. Its significance in anaesthetic practice
6. Phenotypic and molecular biological analysis of human butyrylcholinesterase variants
7. Human serum butyrylcholinesterase and the hydrolysis of succinylcholine
8. On distribution and inheritance of atypical forms of human serum cholinesterase, as indicated by dibucaine numbers
9. DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sites
10. Prolonged response to succinylcholine: A new variant of plasma cholinesterase that is identified as normal by traditional phenotyping methods
11. Voltage dependent calcium channels in adrenal glomerulosa cells and in insulin producing cells