Two missense mutations in SLC26A4 gene: a molecular and functional study
Rebeh, I Ben, Yoshimi, N, Hadj-Kacem, H, Yanohco, S, Hammami, B, Mnif, M, Araki, M, Ghorbel, A, Ayadi, H, Masmoudi, S, Miyazaki, H
Published in Clinical genetics (01.07.2010)
Published in Clinical genetics (01.07.2010)
Get full text
Journal Article
Localization of a Novel Autosomal Recessive Non‐syndromic Hearing Impairment Locus DFNB63 to Chromosome 11q13.3‐q13.4
Tlili, A., Masmoudi, S., Dhouib, H., Bouaziz, S., Rebeh, I. Ben, Chouchen, J., Turki, K., Benzina, Z., Charfedine, I., Drira, M., Ayadi, H.
Published in Annals of human genetics (01.03.2007)
Published in Annals of human genetics (01.03.2007)
Get full text
Journal Article
Identification of mutations underlying 20 inborn errors of metabolism in the United Arab Emirates population
Ben-Rebeh, Imen, Hertecant, Jozef L, Al-Jasmi, Fatma A, Aburawi, Hanan E, Al-Yahyaee, Said A, Al-Gazali, Lihadh, Ali, Bassam R
Published in Genetic testing and molecular biomarkers (01.05.2012)
Published in Genetic testing and molecular biomarkers (01.05.2012)
Get more information
Journal Article