Identification of novel variants in Iranian consanguineous pedigrees with nonsyndromic hearing loss by next‐generation sequencing-Reference-Cited by-同舟云学术

Identification of novel variants in Iranian consanguineous pedigrees with nonsyndromic hearing loss by next‐generation sequencing

Published:2020-08-30 Issue:12 Volume:34 Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

Bitarafan Fatemeh¹^ORCID,Seyedena Seyed Yousef¹,Mahmoudi Mahdi²,Garshasbi Masoud³^ORCID

Affiliation:

1. Department of Biology Faculty of Biological SciencesIslamic Azad University, North Tehran Branch Tehran Iran

2. Rheumatology Research Center Tehran University of Medical Sciences Tehran Iran

3. Department of Medical Genetics Faculty of Medical SciencesTarbiat Modares University Teheran Iran

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry, medical,Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.23544

Reference45 articles.

1. Precision health and deafness–optimizing genetic diagnosis

2. Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations

3. Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran

4. Heterogeneity of hereditary hearing loss in Iran: a comprehensive review;Beheshtian M;Arch Iran Med,2016

5. Hearing loss prevalence and risk factors among Iranian deaf children: The first report from Iran

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