T. Fujisawa

Identification of a point mutation associated with a silent phenotype of human serum butyrylcholinesterase--a case of familial cholinesterasemia.

M. Maeda, N. Sakamoto, K. Hidaka, 1998, Clinica chimica acta; international journal of clinical chemistry.

Suppressor Mutations for Presenilin 1 Familial Alzheimer Disease Mutants Modulate γ-Secretase Activities*

E. Futai, S. Ishiura, T. Tomita, 2015, The Journal of Biological Chemistry.

Identification of missense mutation (G365R) of the butyrylcholinesterase (BCHE) gene in a Japanese patient with familial cholinesterasemia.

Y. Watanabe, K. Sakaguchi, T. Maeda, 2001, The Kobe journal of medical sciences.