H. Lightstone

Phenotypic and molecular biological analysis of human butyrylcholinesterase variants.

C. P. Nogueira, O. Lockridge, C. Bartels, 1990, Clinical biochemistry.

Identification of the structural mutation responsible for the dibucaine-resistant (atypical) variant form of human serum cholinesterase.

C. P. Nogueira, O. Lockridge, C. Bartels, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesterase.

C. P. Nogueira, O. Lockridge, S. Adkins, 1992, American journal of human genetics.

Heterogeneity of the Silent Phenotype of Human Butyrylcholinesterase - Identification of Eight New Mutations

C. Bartels, A. V. D. Spek, B. L. Du, 1992 .

Identification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG).

C. P. Nogueira, O. Lockridge, M. Arpagaus, 1990, American journal of human genetics.

Phenotypic and Molecular Biological Analysis of Butyrylcholinesterase Variants Human

O. Lockridge, A. V. D. Spek, A. Hajra, 1990 .

Characterization of an unstable variant (BChE115D) of human butyrylcholinesterase.

B. La Du, H. Lightstone, S. Primo-Parmo, 1997, Pharmacogenetics.

Phenotypic and Molecular Biological Analysis of Butyrylcholinesterase Variants Human

O. Lockridge, A. Hajra, H. Lightstone, 1990 .