| Literature DB >> 1672297 |
Y Ziv1, G Rotman, M Frydman, J Dagan, T Cohen, T Foroud, R A Gatti, Y Shiloh.
Abstract
The multisystem autosomal recessive disease ataxia-telangiectasia (A-T) is determined by several genes, as evidenced by the existence of four complementation groups in this disorder. Using linkage analysis, the ATA (A-T complementation group A) gene was previously localized to chromosome 11, region q22-q23. Analysis of the segregation of RFLP markers from this region in a Jewish-Moroccan family assigned to group C indicates that the ATC (A-T complementation group C) gene localizes to chromosome 11q22-q23 as well.Entities:
Mesh:
Year: 1991 PMID: 1672297 DOI: 10.1016/0888-7543(91)90268-j
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736