Problem with detection of an insertion-type mutation in the BCHE gene in a patient with butyrylcholinesterase deficiency
Clin Chem
.
2004 Dec;50(12):2410-1.
doi: 10.1373/clinchem.2004.041129.
Authors
Masato Maekawa
1
,
Terumi Taniguchi
,
Jinko Ishikawa
,
Shigeru Toyoda
,
Noriko Takahata
Affiliation
1
Department of Laboratory Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan. mmaekawa@hama-med.ac.jp
PMID:
15563496
DOI:
10.1373/clinchem.2004.041129
No abstract available
Publication types
Case Reports
MeSH terms
Butyrylcholinesterase / deficiency*
Butyrylcholinesterase / genetics*
Child, Preschool
Electrophoresis, Agar Gel
Humans
Male
Mutagenesis, Insertional
Polymerase Chain Reaction
Substances
Butyrylcholinesterase