| Literature DB >> 9004140 |
I Järvelä1, H M Mitchison, P B Munroe, A M O'Rawe, S E Mole, A C Syvänen.
Abstract
Batten disease is the most common progressive neurodegenerative disorder of childhood in western countries. A novel cDNA responsible for Batten disease has recently been identified. We have developed a rapid diagnostic solid phase minisequencing test to detect the major 1.02 kb deletion which is responsible for 81% of affected chromosomes in Batten disease worldwide. In Finland, 90% of Batten chromosomes carry the major deletion owing to the enrichment of the CLN3 gene in the isolated Finnish population.Entities:
Mesh:
Year: 1996 PMID: 9004140 PMCID: PMC1050819 DOI: 10.1136/jmg.33.12.1041
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318