Evidence for a 'silent Allele' GLO0 at the Glyoxalase I Locus
Affiliations
In a three-generation family, the segregation of an apparent silent allele at the GLO I locus in association with the rare HLA haplotype 'AW30-CW4-BW35' was observed in four members. In two cases the assumption of homozygosity at the GLO locus would lead to mother-child exclusions. Phenotypically, the GLO activity in the GLO0 carriers is clearly diminished.
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PMID: 7234136
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PMID: 6885048 DOI: 10.1007/BF00327112.
A new rare variant of the glyoxalase I system of the red cell: GLO-Sicily.
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[A new allele of AK-Polymorphism: AK0 (author's transl)].
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