A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family

Authors:	Afsaneh Taghipour-Sheshdeh Fatemeh Nemati-Zargaran Narges Zarepour Parisa Tahmasebi Nader Saki Mohammad Amin Tabatabaiefar Javad Mohammadi-Asl Morteza Hashemzadeh-Chaleshtori

Institution:	1. Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran;2. Department of Biology, Faculty of Sciences, Ilam University, Ilam, Iran;3. Hearing Research Center, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran;4. Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran;5. Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Noncommunicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran;6. Department of Medical Genetics, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran

Abstract:

Keywords:	Correspondence to: Morteza Hashezadeh-Chaleshtori Cellular and Molecular Research Center Basic Health Sciences Institute Shahrekord University of Medical Sciences Rahmatieh Shahrekord 8813833435 Iran ARNSHL NGS Genetic linkage analysis DFNB loci
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