Screening of 38 Genes Identifies Mutations in 62% of Families with Nonsyndromic Deafness in Turkey-Reference-Cited by-同舟云学术

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Screening of 38 Genes Identifies Mutations in 62% of Families with Nonsyndromic Deafness in Turkey

Published:2011-01 Issue:1-2 Volume:15 Page:29-33
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Duman Duygu¹,Sirmaci Asli²,Cengiz F. Basak¹,Ozdag Hilal³,Tekin Mustafa¹²

Affiliation:

1. Division of Genetics, Department of Pediatrics, Ankara University School of Medicine, Dikimevi, Ankara, Turkey.

2. Dr. John T. Macdonald Department of Human Genetics, John P. Hussman Institute for Human Genomics, Miami, Florida.

3. Biotechnology Institute, Ankara University, Sihhiye, Ankara, Turkey.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2010.0120

Reference32 articles.

1. Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

2. Screening of the DFNB3 Locus: Identification of Three Novel Mutations of MYO15A Associated with Hearing Loss and Further Suggestion for Two Distinctive Genes on This Locus

3. Interactive visual analysis of SNP data for rapid autozygosity mapping in consanguineous families

4. Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population

5. Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan

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1. Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia;Annals of Human Genetics;2024-03-22

2. Recent advances in genetic etiology of non-syndromic deafness in children;Frontiers in Neuroscience;2023-10-19

3. The natural history, clinical outcomes, and genotype–phenotype relationship of otoferlin-related hearing loss: a systematic, quantitative literature review;Human Genetics;2023-09-07

4. Preservation of Distortion Product Otoacoustic Emissions in OTOF-Related Hearing Impairment;Ear & Hearing;2023-09-06

5. Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families;Human Genomics;2023-05-15

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