| Literature DB >> 2272147 |
M Hamza1, K Ayed, R Bardi, L Gebuhrer, H Betuel, T Bardin, R Plaetke, M Lathrop.
Abstract
Thirty members of a Tunisian family with hereditary chondrocalcinosis were typed for HLA-A, B, and DR antigens: 7 affected and 23 unaffected subjects in three consecutive generations. The haplotype A1 B12 DR3 was found in all affected subjects and in 8 unaffected members. Chondrocalcinosis in this family may be associated with the haplotype A1 B12 DR3. The mode of transmission was autosomal dominant with incomplete penetrance.Entities:
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Year: 1990 PMID: 2272147
Source DB: PubMed Journal: Dis Markers ISSN: 0278-0240 Impact factor: 3.434