Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21

Citation
Se. Antonarakis et al., Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21, AM J MED G, 88(4), 1999, pp. 348-351
Citations number
17
Categorie Soggetti
Molecular Biology & Genetics
Journal title
AMERICAN JOURNAL OF MEDICAL GENETICS
ISSN journal
01487299 → ACNP
Volume
88
Issue
4
Year of publication
1999
Pages
348 - 351
Database
ISI
SICI code
0148-7299(19990820)88:4<348:LOLOAB>2.0.ZU;2-4
Abstract
To determine the importance of a candidate gene KCNN3 (formerly named hSKCa 3) in the susceptibility to schizophrenia, we have studied the genotypes of a (CAG)n polymorphism within this gene in the DNAs of the members of 54 mu ltiplex families with this disease, Parametric and nonparametric linkage an alysis did not provide evidence for linkage between KCNN3 (that we mapped t o chromosome 1q21) and schizophrenia. Furthermore, we observed no differenc e in the distribution of the (CAG)n alleles between affected and normal ind ividuals. These results: do not support the hypothesis that larger KCNN3 al leles are preferentially associated with schizophrenia [Chandy et al. 1998 Mol Psychiatr 3:32-37] in individuals from multiply affected families. Amer , J. Med, Genet, (Neuropsychiatr. Genet,) 88:348-351, 1999, (C) 1999:Wiley- Liss, Inc.