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ACP1 Polymorphism: Five New Variants Detected by Multiple Electrophoretic Methods

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Advances in Forensic Haemogenetics

Part of the book series: Advances in Forensic Haemogenetics ((HAEMOGENETICS,volume 2))

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Abstract

Human red cell acid phosphatase (ACP1, EC 3.1.3.2) is known to be genetically polymorphic. Three codominant autosomal alleles ACP1*A,B and C were first described by Hopkinson (1963) using differences in electrophoretic mobilities. Other variants published to date include ACP1*D, E, F, G. H, I, K, M, R, GUA-1 and TIC-1. This report describes five new variants identified by both isoelectric focusing and conventional electrophoresis. The new alleles show genetic transmission from family data and are named ACP1*N, P, S, T, and U. Further evidence of an allele with reversed ACP1 A band intensity and a variant with reduced ACP1 C activity are discussed.

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© 1988 Springer-Verlag Berlin Heidelberg

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Miller, S.A., Dykes, D.D., Polesky, H.F. (1988). ACP1 Polymorphism: Five New Variants Detected by Multiple Electrophoretic Methods. In: Mayr, W.R. (eds) Advances in Forensic Haemogenetics. Advances in Forensic Haemogenetics, vol 2. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-73330-7_18

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  • DOI: https://doi.org/10.1007/978-3-642-73330-7_18

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-18765-3

  • Online ISBN: 978-3-642-73330-7

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