| Literature DB >> 669712 |
Abstract
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.Entities:
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Year: 1978 PMID: 669712 DOI: 10.1007/BF00291312
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132