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Part of the book series: Advances in Forensic Haemogenetics ((HAEMOGENETICS,volume 1))

Abstract

The polymorphism of human esterase D (ESD) was first detected 1973 (1) with three common phenotypes, determined by two autosomal codominant alleles, ESD*1 and ESD*2. Other investigators described some rare alleles ESD*3 (2), ESD*4 (3), ESD*6 (4), ESD*7 (5), ESD*Cph (6), ESD*D (7), and the common allele ESD*5 (8). There is evidence for the existence of a silent allele ESD*0 (9,10) and a variation of activity between phenotypes(11).

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© 1986 Springer-Verlag Berlin Heidelberg

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Gradl, G., Weidinger, S., Cleve, H., Schwarzfischer, F. (1986). Genetic Study of Red Cell Esterase D Polymorphism by Isoelectric Focusing. In: Brinkmann, B., Henningsen, K. (eds) 11th Congress of the Society for Forensic Haemogenetics (Gesellschaft für forensische Blutgruppenkunde e.V.). Advances in Forensic Haemogenetics, vol 1. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-71150-3_36

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  • DOI: https://doi.org/10.1007/978-3-642-71150-3_36

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-16500-2

  • Online ISBN: 978-3-642-71150-3

  • eBook Packages: Springer Book Archive

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