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- W2040271000 abstract "A case of complete deficiency of lactate dehydrogenase subunit H is presented. The abnormality is presumably hereditary. A 64-year-old male with mild diabetes drew our attention because of the abnormally low lactate dehydrogenase activity in the serum (77 mIU/ml). The analysis of serum, hemolysate and saliva demonstrated only M4 isoenzyme, lacking the faster moving fraction. A similar study made on family members revealed low lactate dehydrogenase activity in their serum also linked with decreased relative activity of the H4 fraction. Based on the comparison of the calculated ratio of H/M subunits in normal and affected family members, it was hypothesized that the proband is homozygous and the affected family members are heterozygous. Such a result would strongly suggest that the reported deficiency of subunit H has a hereditary basis." @default.
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- W2040271000 date "1971-10-01" @default.
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- W2040271000 title "Hereditary deficiency of subunit H of lactate dehydrogenase" @default.
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- W2040271000 doi "https://doi.org/10.1016/0009-8981(71)90095-7" @default.
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