Confirmation of linkage of Sjögren-Larsson syndrome to chromosome 17 in families of different ethnic origins.
case_control · Level III
Where this comes from
- Record sourced from PubMed, PMID 8728707.
- Also identified by PMC identifier 1051883.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Linkage analysis in two consanguineous pedigrees of Pakistani and English origin and one further Indian family in which affected subjects have Sjögren-Larsson syndrome (SLS) showed linkage to chromosome 17. Linkage of SLS to D17S783 and D17S805 has been reported in Swedish pedigrees, but since those data were generated from a single ethnic group originating from a common ancestor, there remained the question of whether this disease is genetically heterogeneous. This report confirms the linkage in non-Swedish pedigrees and, therefore, provides evidence to support a single locus for SLS.
Medical subject headings
- Chromosomes, Human, Pair 17
- Sjogren-Larsson Syndrome