Nonsense mutation in exon 2 of the butyrylcholinesterase gene: a case of familial cholinesterasemia

Author:

Hidaka Kazuo,Iuchi Iwao,Yamasaki Toshiko,Ueda Naoki,Hukano Kouichi

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference14 articles.

1. Complete amino acid sequence of human serum cholinesterase;Lockridge;J Biol Chem,1987

2. Cholinesterase and anticholinesterases;Pantzuck,1975

3. Inactivation of the cholinesterase gene by Alu insertion: possible mechanism for human gene transposition;Muratani,1991

4. Identification of two different genetic mutations associated with phenotypes for human serum cholinesterase in Japanese;Hidaka;J Clin Pathol,1992

5. Genetic basis of the silent phenotype of serum butyrylcholinesterase in three compound heterozygotes;Maekawa;Clin Chim Acta,1995

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