Evidence for a 'silent allele' GLO0 at the glyoxalase I locus.
作者： Ch. Rittner , W. Weber
DOI: 10.1007/BF00291312
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摘要: In a three-generation family, the segregation of an apparent silent allele at GLO I locus in association with rare HLA haplotype ‘AW30-CW4-BW35’ was observed four members. two cases assumption homozygosity would lead to mother-child exclusions. Phenotypically, activity GLO0 carriers is clearly diminished.
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sci-hub.se 参考文章(8)
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