Heterogeneity of the Silent Phenotype of Human Butyrylcholinesterase - Identification of Eight New Mutations
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Publisher
Springer US
Link
http://link.springer.com/content/pdf/10.1007/978-1-4615-3046-6_8
Reference13 articles.
1. Arpagaus, M., Kott, M., Vatsis, K.P., Bartels, C.F., La Du, B.N. and Lockridge, O., 1990, Structure of the gene for human butyryicholinesterase. Evidence for a single copy, Biochemistry 29:124.
2. Goedde, H.W. and Altland, K., 1968, Evidence for different silent genes in the human serum cholinesterase polymorphism, Ann. N.Y. Acad. Sci. 151:540.
3. Harris, H. and Whittaker, M., 1961, Differential inhibition of human serum cholinesterase with fluoride:recognition of two new phenotypes, Nature 191:496.
4. Kalow, W. and Genest, K., 1957, A method for the detection of atypical forms of human cholinesterase:determination of dibucaine numbers, Can. J. Biochem. 35:339.
5. La Du, B.N., Bartels, C.F., Nogueira, C.D., Arpagaus, M. and Lockridge, O., 1991, Proposed nomenclature for human butyryicholinesterase genetic variants identified by DNA sequencing, Cell. Mol. Neurobiol. 11:79.
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