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Identification of a point mutation associated with a silent phenotype of human serum butyrylcholinesterase – a case of familial cholinesterasemia
Norikazu Sakamoto, Kazuo Hidaka, Takashi Fujisawa, Mitsuo Maeda, Iwao IuchiVolume:
274
Year:
1998
Language:
english
DOI:
10.1016/s0009-8981(98)00058-8
File:
PDF, 171 KB
english, 1998