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dc.contributor.authorBwibo, N. O.
dc.contributor.authorBeutler, E.
dc.contributor.authorChern, CJ,
dc.date.accessioned2013-07-19T09:45:35Z
dc.date.available2013-07-19T09:45:35Z
dc.date.issued1976
dc.identifier.citationChern, CJ, Beutler E. 1976. Biochemical and electrophoretic studies of erythrocyte pyridoxine kinase in white and black Americans., 1976 Jan. American journal of human genetics. 28(1):9-17.en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/49401
dc.description.abstractThe mean PNK activity in red blood cells from black subjects was only about 40% of that in whites. Among 51 whites examined, one was found to have enzyme deficiency. The estimated gene frequencies for PNKH (the common allele in whites which codes for higher enzyme activity) and PNKL (the common allele in blacks which codes for lower enzyme activity) were .35 and .65, respectively, for black donors, and .81 and .19, respectively, for white donors, The variant enzyme in persons with enzyme deficiency was associated with an increased rate of degradation in red cells during aging. No other biochemical or electrophoretic differences were detected.en
dc.language.isoenen
dc.titleBiochemical and electrophoretic studies of erythrocyte pyridoxine kinase in white and black Americans.en
dc.typeArticleen
local.publisherDept. of Paediatrics and Child Health, University of Nairobi.en


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