Abstract
Human S-adenosylhomocysteine hydrolase (AHCY; EC 3.3.1.1) exhibits a genetic polymorphism first described by Bissbort et al. (1983) who demonstrated the occurrence of two common electrophoretic phenotypes (AHCY 1 and AHCY 2−1) determined by two codominant alleles (AHCY*1 and AHCY*2) at an autosomal locus.
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References
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© 1990 Springer-Verlag Berlin Heidelberg
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Rocha, J., Bento, C., Veiga, I., Amorim, A. (1990). Biochemical and population genetics of S-adenosylhomocysteine hydrolase in NW Portugal. In: Polesky, H.F., Mayr, W.R. (eds) 13th Congress of the International Society for Forensic Haemogenetics (Internationale Gesellschaft für forensische Hämogenetik e.V.) New Orleans, October 19–21, 1989. Advances in Forensic Haemogenetics, vol 3. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-75496-8_68
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DOI: https://doi.org/10.1007/978-3-642-75496-8_68
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