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Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss.
Mkaouar-Rebai E, Tlili A, Masmoudi S, Louhichi N, Charfeddine I, Ben Amor M, Lahmar I, Driss N, Drira M, Ayadi H, Fakhfakh F. Mkaouar-Rebai E, et al. Among authors: charfeddine i. Biochem Biophys Res Commun. 2006 Feb 24;340(4):1251-8. doi: 10.1016/j.bbrc.2005.12.123. Epub 2006 Jan 5. Biochem Biophys Res Commun. 2006. PMID: 16406239 Clinical Trial.
Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutation.
Belguith H, Hajji S, Salem N, Charfeddine I, Lahmar I, Amor MB, Ouldim K, Chouery E, Driss N, Drira M, Mégarbané A, Rebai A, Sefiani A, Masmoudi S, Ayadi H. Belguith H, et al. Among authors: charfeddine i. Clin Genet. 2005 Aug;68(2):188-9. doi: 10.1111/j.1399-0004.2005.00474.x. Clin Genet. 2005. PMID: 15996220 No abstract available.
SLC26A4 variations among Graves' hyper-functioning thyroid gland.
Hadj-Kacem H, Kallel R, Belguith-Maalej S, Mnif M, Charfeddine I, Ghorbel A, Abid M, Ayadi H, Masmoudi S. Hadj-Kacem H, et al. Among authors: charfeddine i. Dis Markers. 2010;29(2):63-9. doi: 10.3233/DMA-2010-0727. Dis Markers. 2010. PMID: 21045265 Free PMC article.
105 results