Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran

Author:

Mohseni Marzieh1ORCID,Babanejad Mojgan1ORCID,Booth Kevin T.23,Jamali Payman4,Jalalvand Khadijeh1,Davarnia Behzad5,Ardalani Fariba1,Khoshaeen Atefeh6,Arzhangi Sanaz1,Ghodratpour Fatemeh1,Beheshtian Maryam1,Jahanshad Faezeh7,Otukesh Hasan8,Bahrami Fatemeh1,Seifati Seyed Morteza9,Bazazzadegan Niloofar1,Habibi Farkhonde10,Behravan Hanieh1,Mirzaei Sepide1,Keshavarzi Fatemeh1,Nikzat Nooshin1,Mehrjoo Zohreh1,Thiele Holger11,Nothnagel Michael1112ORCID,Azaiez Hela2,Smith Richard J.2ORCID,Kahrizi Kimia1ORCID,Najmabadi Hossein1ORCID

Affiliation:

1. Genetics Research Center University of Social Welfare and Rehabilitation Sciences Tehran Iran

2. Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology, Carver College of Medicine University of Iowa Iowa City Iowa USA

3. Department of Neurobiology Harvard Medical School Boston Massachusetts USA

4. Shahrood Genetic Counseling Center Welfare Organization Semnan Iran

5. Department of Anatomy and Pathology Ardabil University of Medical Sciences Ardabil Iran

6. Mehrgan Genetic Clinic Sari Iran

7. Navid's Institute of Infertility Tehran Iran

8. Department of Pediatric Neurology Iran University of Medical Sciences Tehran Iran

9. Medical Biotechnology Research Center Islamic Azad University Ashkezar Iran

10. Genetic Counseling Center of Welfare Organization Rasht Iran

11. Cologne Center for Genomics (CCG) University of Cologne Cologne Germany

12. University Hospital Cologne Cologne Germany

Funder

Iran National Science Foundation

National Institute for Medical Research Development

National Institute of General Medical Sciences

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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