High Frequency of the p.R34X Mutation in the TMC1 Gene Associated with Nonsyndromic Hearing Loss Is Due to Founder Effects

Author:

Saïd Mariem Ben1,Hmani-Aifa Mounira1,Amar Imen12,Baig Shahid Mahmood3,Mustapha Mirna45,Delmaghani Sedigheh6,Tlili Abdelaziz1,Ghorbel Abdelmonem7,Ayadi Hammadi1,Van Camp Guy8,Smith Richard J.H.9,Tekin Mustafa1011,Masmoudi Saber1

Affiliation:

1. Targets for Diagnosis and Therapy Unit, Centre of Biotechnology of Sfax, Sfax, Tunisia.

2. Laboratory of Genetics, Faculty of Biological Sciences, USTHB, El-Alia, Algeria.

3. Human Molecular Genetics Laboratory, Health Biotechnology Division, NIBGE, Faisalabad, Pakistan.

4. Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan.

5. Department of Otolaryngology, Stanford University School of Medicine, Stanford, California.

6. Unit of Genetics and Physiology of Hearing, INSERM U587, Pasteur Institute, Paris, France.

7. Department of Otolaryngology, C.H.U.H. Bourguiba of Sfax, Sfax, Tunisia.

8. Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.

9. Molecular Otolaryngology Research Laboratories, Department of Otolaryngology, University of Iowa, Iowa City, Iowa.

10. Division of Clinical Molecular Pathology and Genetics, Department of Pediatrics, Ankara University School of Medicine, Ankara, Turkey.

11. Dr. John T. MacDonald Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, Florida.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

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