The K variant of human butyrylcholinesterase is caused by a G/A transition in the butyrylcholinesterase gene, which neither creates nor destroys any restriction site. In an attempt to detect the K variant both simply and rapidly, we developed a two step method of ''PCR primer introduced restriction analysis'' (PCR-PIRA). The first step was used to introduce a new Fun4HI site into the normal allele for a screening test, while the second step was performed to create a new MaeIII site on the variant allele for a specific test. This method thus enabled us to distinguish clearly the K variant from the normal allele, and also showed that the frequency of the K variant allele is 0.164 in the Japanese population.
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Univ Monastir, Fac Pharm, Res Unit Biol & Mol Anthropol Appl Dev & Hlth, Monastir, TunisiaUniv Monastir, Fac Pharm, Res Unit Biol & Mol Anthropol Appl Dev & Hlth, Monastir, Tunisia
Denden, S.
Abaidi, H.
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Univ Tunis El Manar, Ecole Super Sci & Tech Sante Tunis, Res Unit Antioxidant Cpds Oxidat Str Trace Elemen, Tunis, TunisiaUniv Monastir, Fac Pharm, Res Unit Biol & Mol Anthropol Appl Dev & Hlth, Monastir, Tunisia
Abaidi, H.
Hamdaoui, M. H.
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Univ Tunis El Manar, Ecole Super Sci & Tech Sante Tunis, Res Unit Antioxidant Cpds Oxidat Str Trace Elemen, Tunis, TunisiaUniv Monastir, Fac Pharm, Res Unit Biol & Mol Anthropol Appl Dev & Hlth, Monastir, Tunisia
Hamdaoui, M. H.
Ben Chibani, J.
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Univ Monastir, Fac Pharm, Res Unit Biol & Mol Anthropol Appl Dev & Hlth, Monastir, TunisiaUniv Monastir, Fac Pharm, Res Unit Biol & Mol Anthropol Appl Dev & Hlth, Monastir, Tunisia
Ben Chibani, J.
Khelil, A. Haj
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Univ Monastir, Fac Pharm, Res Unit Biol & Mol Anthropol Appl Dev & Hlth, Monastir, TunisiaUniv Monastir, Fac Pharm, Res Unit Biol & Mol Anthropol Appl Dev & Hlth, Monastir, Tunisia