Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss-Reference-Cited by-同舟云学术

Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss

Published:2006-02 Issue:4 Volume:340 Page:1251-1258
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Mkaouar-Rebai Emna,Tlili Abdelaziz,Masmoudi Saber,Louhichi Nacim,Charfeddine Ilhem,Amor Mohamed Ben,Lahmar Imed,Driss Nabil,Drira Mohamed,Ayadi Hammadi,Fakhfakh Faiza

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference33 articles.

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4. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides;Estivill;Am. J. Hum. Genet.,1998

5. Hearing loss due to the mitochondrial A1555G mutation in Italian families;Casano;Am. J. Med. Genet.,1998

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