DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sites

American Journal of Human Genetics

Volumn 50, Issue 5, 1992, Pages 1086-1103

  Bartels, C F ^a   Jensen, F S ^a   Lockridge, O ^a   Van der Spek, A F L ^a   Rubinstein, H M ^a   Lubrano, T ^a   La Du, B N ^a  

^a UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHOLINESTERASE; ENZYME VARIANT; SUXAMETHONIUM;

AMINO ACID SUBSTITUTION; ARTICLE; CONTROLLED STUDY; DNA DETERMINATION; DNA POLYMORPHISM; DNA SEQUENCE; ENZYME ACTIVITY; ENZYME STABILITY; GENE MUTATION; GENETIC LINKAGE; GENETIC VARIABILITY; GENOTYPE; HUMAN; HUMAN CELL; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; BASE SEQUENCE; BUTYRYLCHOLINESTERASE; FEMALE; HUMAN; LINKAGE (GENETICS); MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM (GENETICS); SUPPORT, U.S. GOV'T, P.H.S.; TEMPERATURE; VARIATION (GENETICS);

EID: 0026695539     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)