RLIP76 GENE VARIANTS ARE NOT ASSOCIATED WITH
DRUG RESPONSE IN TURKISH EPILEPSY PATIENTS Manguoğlu E1,*, Akdeniz S1, Dündar NO2, Duman Ö2,
Aktekin B3, Haspolat Ş2, Bilge U4, Özel D4, Lüleci G1 *Corresponding Author: Esra Manguoğlu, Department of Medical Biology and Genetics, Faculty of Medicine,
Akdeniz University, Antalya, Turkey;
Tel.: +90-242-249-6977; Fax: +90-242-249-6906; E-mail: emanguoglu@akdeniz.edu.tr page: 25
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RESULTS
We have not detected any sequence change in
the coding regions of the gene. However, two substitutions
within the 5’UTR (5’ untranslated region)
(c.160-4G>A, c.187 C>G); eight substitutions within
the intronic regions (c.1562-38G>A, c.1670+107G>A,
c.1670+93G>A, c.1670+96G>A, c.1670+100C>T,
c.1670+130C>T, c.1670+131G>C, c.1670+140G>C)
were detected. The c.187G>C change was detected
in two refractory and one non refractory patients, the
c.1670+93G>A change was detected in four refractory
and six non refractory patients, the c.1670+96G>A
and c.1670+100C>T changes were detected in one refractory
patient and the c.1670+131G>C and c.1670+
140G>C changes in one non refractory patient each.
Allele frequencies and statistical analyses results for
all sequence changes are presented in Table 2. Allele
distributions that were analyzed with regard to age (p
0.774, Pearson χ2 analysis), gender (p 0.433, Pearson
χ2 Chi-Square analysis), drug response status and allele
frequencies revealed no statistically significant
correlation.
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